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Automated assessment of biological database assertions using the scientific literature



The large biological databases such as GenBank contain vast numbers of records, the content of which is substantively based on external resources, including published literature. Manual curation is used to establish whether the literature and the records are indeed consistent. We explore in this paper an automated method for assessing the consistency of biological assertions, to assist biocurators, which we call BARC, Biocuration tool for Assessment of Relation Consistency. In this method a biological assertion is represented as a relation between two objects (for example, a gene and a disease); we then use our novel set-based relevance algorithm SaBRA to retrieve pertinent literature, and apply a classifier to estimate the likelihood that this relation (assertion) is correct.


Our experiments on assessing gene–disease relations and protein–protein interactions using the PubMed Central collection show that BARC can be effective at assisting curators to perform data cleansing. Specifically, the results obtained showed that BARC substantially outperforms the best baselines, with an improvement of F-measure of 3.5% and 13%, respectively, on gene-disease relations and protein-protein interactions. We have additionally carried out a feature analysis that showed that all feature types are informative, as are all fields of the documents.


BARC provides a clear benefit for the biocuration community, as there are no prior automated tools for identifying inconsistent assertions in large-scale biological databases.


The large biological databases are a foundational, critical resource in both biomedical research and, increasingly, clinical health practice. These databases, typified by GenBankFootnote 1 and UniProt,Footnote 2 represent our collective knowledge of DNA and RNA sequences, genes, proteins, and other kinds of biological entities. The main databases currently contain hundreds of millions of records, each directly or indirectly based on scientific literature or material produced by a reputable laboratory. Each record is contributed by an individual research team, or is derived indirectly from such a contribution, and thus the contents of these databases represent decades of manual effort by the global biomedical community. The databases are used by researchers to infer biological properties of organisms, and by clinicians in disease diagnosis and genetic assessment of health risk [1].

Manual biocuration is used with some of the databases to ensure that their contents are correct [2]. Biocuration consists of organizing, integrating, and annotating biological data, with the primary aim of ensuring that the data is reliably retrievable. Specifically, a biocurator derives facts and assertions about biological data, and then verifies their consistency in relevant publications. PubMedFootnote 3 [3], as the primary index of biomedical research publications, is typically consulted for this purpose.

For example, given a database record with the assertion “the BRCA gene is involved in Alzheimer’s disease”, a biocurator may search for articles that support or deny that assertion, typically via a PubMed keyword search, and then manually review the articles to confirm the information. Biocuration is, therefore, time-consuming and expensive [4, 5]; curation of a single protein may take up to a week and requires considerable human investment both in terms of knowledge and effort [6].

However, biological databases such as GenBank or UniProt contain hundreds of millions of uncurated nucleic acid and protein sequence records [7], which suffer from a large range of data quality issues including errors, discrepancies, redundancies, ambiguities, and incompleteness [8, 9]. Exhaustive curation on this scale is utterly infeasible; most error detection occurs when submitters re-examine their own records, or occasionally when reported by a user, but it is likely that the rate of error detection is low. Figure 1 illustrates the growth of the curated database UniProtKB/Swiss-Prot against the growth of the uncurated database UniProtKB/TrEMBL (which now contains roughly 89M records). Given the huge gap shown in Fig. 1, it is clear that automated and semi-automated error-detection methods are needed to help and assist biocurators to provide reliable biological data to the research community [10, 11].

Fig. 1

Growth of the number of sequences in UniProt databases. The green and pink lines shows the growth in UniProtKB for TrEMBL and Swiss-Prot respectively entries from January 2012 to January of 2019. The sharp drop in TrEMBL entries corresponds to a proteome redundancy minimization procedure implemented in March 2015 [5]. a Growth of TrEMBL. b Growth of Swiss-Prot

In this work, we seek to use the literature to develop an automated method for assessing the consistency of biological assertions. This research builds on our previous work, in which we used the scientific literature to detect biological sequences that may be incorrect [12], to detect literature-inconsistent sequences [13], and to identify biological sequence types [14]. In our previous work on data quality in biological databases, we formalized the quality problem as a characteristic of queries (derived from record definitions); in the discipline of information retrieval there are metrics for estimating query quality. In contrast, in this work we consider the consistency of biological assertions. Previously, we formalized the problem as a pure information retrieval problem, whereas here we also consider linguistic features.

To demonstrate the scale of the challenge we address in this paper, consider Fig. 2, which shows the distribution of literature co-mentions (co-occurrences) of correct or incorrect gene–disease relations and correct or incorrect protein–protein interactions, where correctness is determined based on human-curated relational data (described further in “Experimental data” section). For example, a gene–disease relation represents an assertion of the form Gene–Relation–Disease, where Relation is a predicate representing the relationship between the gene and the disease, such as “causes”, “involved in”, or “related to”. This analysis shows that, despite the fact that entities that are arguments of correct relations tend to be co-mentioned more often than those in incorrect relations, simplistic filtering methods based on a frequency threshold are unlikely to be effective at distinguishing correct from incorrect relations. Moreover, for many incorrect relations, the entities that are arguments of the relation are often mentioned together in a text (co-mentioned) despite not being formally related. Therefore, more sophisticated techniques are needed to address this problem.

Fig. 2

Distribution of co-mention frequencies for in/correct relations described in “Experimental data” section. It is apparent that even when two entities are not known to have a valid relationship (an incorrect relation), these entities may often be mentioned together in a text (co-mentioned)

We have developed BARC, a Biocuration tool for Assessment of Relation Consistency.Footnote 4 In BARC, a biological assertion is represented as a relation between two entities (such as a gene and a disease), and is assessed in a three-step process. First, for a given pair of objects (object1,object2) involved in a relation, BARC retrieves a subset of documents that are relevant to that relation using SaBRA, a document ranking algorithm we have developed. The algorithm is based on the notion of the relevant set rather than an individual relevant document. Second, the set of retrieved documents is aggregated to enable extraction of relevant features to characterise the relation. Third, BARC uses a classifier to estimate the likelihood that this assertion is correct. The contributions of this paper are as follows:

  1. 1

    We develop a method that uses the scientific literature to estimate the likelihood of correctness of biological assertions.

  2. 2

    We propose and evaluate SaBRA, a ranking algorithm for retrieving document sets rather than individual documents.

  3. 3

    We present an experimental evaluation using assertions representing gene–disease relations and protein–protein interactions on the PubMed Central Collection, where BARC achieved, respectively, 89% and 79% of accuracy.

Our results show that BARC, which compiles and integrates the methods and algorithms developed in this paper, outperforms plausible baselines across all metrics, on a dataset of several thousand assertions evaluated against a repository of over one million full-text publications.

Problem definition

Biocuration can be defined as the transformation of biological data into an organized form [2]. To achieve this, a biocurator typically manually reviews published literature to identify assertions related to entities of interest with the goal of enriching a curated database, such as UniProtKB/Swiss-Prot. However, there are also large databases of uncurated information, such as UniProtKB/TrEMBL, and biocurators would also need to check the assertions within these databases for their veracity, again with respect to the literature. Biological assertions that biocurators check are of various types. For example, they include:

  • Genotype-phenotype relations (OMIM db): these include assertions about gene–disease relations or mutation-disease or gene-disease relations [15]. A biocurator will then have to answer questions such as: “is the BRCA gene involved in Alzheimer’s disease?

  • Functional residue in protein (Catalytic Site Atlas or BindingMOAD databases): these include assertions about sub-sequences being a functional residue of a given protein [16, 17]. An example question is: “is Tyr247 a functional residue in cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA)?

  • Protein-protein interaction (BioGRID db): these include assertions about interactions between proteins. An example question is: “is the protein phosphatase PPH3 related to the protein PP2A?” [18].

  • Drug-treats-disease (PharmGKB database): which includes assertions about a drug being a treatment of a disease. An example question is: “can Tamoxifen be used to treat AtopyFootnote 5?” [19].

  • Drug-causes-disease (CTD database): these include assertions about drugs causing a disease [20]. An example question is: “can paracetamol induce liver disease?”.

The biocuration task is time-consuming and requires a considerable investment in terms of knowledge and human effort. A supportive tool has the potential to save significant time and effort.

In this work, we focus on the analysis of only two type of relations, namely gene-disease and gene-gene relations. We leave the analysis of other relations to future work.

We propose to represent and model a relation, defined as follows:

Definition 1

Let O1 and O2 be respectively a set of objects of type 1 and a set of objects of type 2. A relationR is a triplet of the form (object1,predicate,object2), where object1O1 and object2O2 are entities that have some relationship between them as indicated by the predicate.

For example, the assertion “The gene CFTR causes the disease cystic fibrosis” is represented by the gene–disease relation R:

R=(CFTR,causes,Cystic fibrosis) where CFTR is of type gene and Cystic fibrosis is of type disease.

Note that the transformation of an assertion from its linguistic declarative form to the relational form is undertaken by the biocurator, and is out of the scope of this paper.

We formally define the problem we study as follows. Given

  • A collection of documents that represents the domain literature knowledge D=<d1,d2,…,dk>;

  • A set of n relation types T={T1,T2,...,Tn}, where RmTn defines a relation between two objects that holds in the context of the assertion type Tn;

  • A set of annotated relations \(R_{T_{n}}\) for a particular assertion type Tn such as \(R_{T_{n}}=<(R_{1},y_{1}),(R_{2},y_{2}),\ldots,(R_{m},y_{m})>\), where RmTn and ym{correct,incorrect};

we aim to classify a new and unseen relation Rp of type Tl as being correct or incorrect given the domain literature knowledge D. In other words, we seek support for that assertion in the scientific literature. The resulting tool described in the next sections is expected to be used at curation time.


Figure 3 describes the logical architecture of our tool, BARC, a Biocuration tool for Assessment of Relation Consistency. The method embodied in BARC uses machine learning, and thus relies on a two-step process of learning and predicting. At the core of BARC are three components that we now describe.

Fig. 3

Architecture overview of BARC

Retrieval (“SaBRA” section): This component handles the tasks of processing a relation and collecting a subset of the documents that are used to assess the validity of that assertion. The inputs of this component are a relation and the document index built for the search task. The internal search and ranking algorithm implemented by this component is described later. Indexing of the collection is out of the scope of this paper, but is briefly reviewed in “Experimental data” section.

Aggregation & feature extraction (“Relation consistency features” section): This component takes as an input the set of documents returned by the retrieval component and is responsible for the main task of aggregating this set of documents to allow extraction of relevant features. Three kinds of features are then computed and produced, (i) inferred relation words, (ii) co-mention based, and (iii) context similarity-based. These features are discussed in “Relation consistency features” section.

Learning and prediction (“Supervised learning algorithm” section): This component is the machine-learning core of BARC. It takes as input feature vectors, each representing a particular relation. These feature vectors are processed by two sub-components depending on the task: the learning pipeline and the prediction pipeline. The learning pipeline is responsible for the creation of a model, which is then used by the prediction pipeline to classify unseen assertions as being correct or incorrect.

SaBRA for ranking documents

In typical information retrieval applications, the objective is to return lists of documents from a given document collection, ranked by their relevancy to a user’s query. In the case of BARC, the documents being retrieved are not intended for individual consideration by a user, but rather with the purpose of aggregating them for feature extraction for our classification task. Hence, given a relation R=(object1,predicate,object2), we need to select documents that mention both object1 and object2 at a suitable ratio, to allow accurate computation of features; a set of documents that is biased towards documents containing either object1 or object2 will result in low-quality features. Standard IR models such as the vector-space model TF-IDF [21] or the probabilistic model BM25 [22] are not designed to satisfy this constraint.

Given the settings and the problem discussed above, we developed SaBRA, a Set-Based Retrieval Algorithm, as summarized in Algorithm 1. In brief, SaBRA is designed to guarantee the presence of a reasonable ratio of mentions for object1 and object2 in the top k documents retrieved, to extract features for a relation R=(object1,predicate,object2).

SaBRA takes in input an IndexSearcher that implements search over a single index, a query in the form of a relation assertion R=(o1,p,o2), where k the number of documents to return (choice of k is examined later). First, SaBRA initializes three empty ordered lists ζ, θ1, and θ2 (line 1; these sets are explained below), and sets the similarity function the IndexSearch used (line 2). Given a relation R and a document d, the scoring function used to compute the similarity is the following:

$$ {\begin{aligned} {}{f(R,d)=\frac{\log[1+count(o_{1},d)]}{(1-b)+b\times|d|_{o_{1}}}+\frac{\log[1+count(o_{2},d)]}{(1-b)+b\times|d|_{o_{2}}}} \end{aligned}} $$

where count(o,d) is the number of time o occurs in d, the value |d|o is the number of mentions of objects of the same type as o in document d, and b is a weighting parameter empirically determined and set to 0.75 in our experiments. The intuition behind the denominator for the two terms is to penalize documents that mention other objects of the same type as o [23], such as other genes or diseases other than those involved in the relational assertion being processed. The numerator acts provides term frequency weighting.

Next, SaBRA retrieves: (i) documents that mention both o1 and o2 in the ordered list ζ (line 3), (ii) documents that mention o1 but not o2 in the ordered list θ1 (line 4), and (iii) documents that mention o2 but not o1 in the ordered list θ2 (line 5). Then, SaBRA alternately inserts documents of θ1 and θ2 at the end of ζ (lines 6 to 13). Documents in ζ are considered to be more significant as they contain documents that mention and may link the two objects involved in the relation being processed. Finally, SaBRA returns the top-k documents of the ordered list ζ(line 14).

Relation consistency features

We now explain the features that BARC extracts from the set of documents retrieved by its retrieval component through SaBRA.

Inferred relation word features

Given a correct relation R=(object1,predicate,object2), we expect that object1 and object2 will co-occur in sentences in the scientific literature (co-mentions), and that words expressing the predicate of the target relation between them will also occur in those sentences. This assumption is commonly adopted in resources for and approaches to relation extraction from the literature, such as in the HPRD corpus [24, 25]. Following this intuition, we have automatically analyzed correct relations of the training set described in “Experimental data” section to extract words that occur in all sentences where the two objects of each correct relation are co-mentioned. Tables 1 and 2 show the top 5 co-occurring words for the correct relations we have considered, their frequencies across all sentences, and example sentences in which the words co-occur with the two objects involved in a relevant relation in the data set. For example, the most common word that occurs with gene–disease pairs is the word “mutation”; it may suggest the relation between them. These words can be considered to represent the relation predicate R. Hence, these inferred relation word features can capture the predicate.

Table 1 Examples of the top 5 words that occur in sentences where genes and diseases of the relations described in “Experimental data” section also occur
Table 2 Examples of the top 5 words that occur in sentences where two proteins that interact also occur

For each relation type we have curated a list of the top 100 co-occurring words as described above. Then, for each relation R=(object1,predicate,object2) of type T, a feature vector is defined with values representing the frequency of appearance of that word in sentences where object1 and object2 occur. Hence, our model will inherently succeed in capturing different predicates between the same pair of objects. We separately consider the three different fields of the documents (title, abstract and body). In total, we obtain 300 word-level features for these inferred relation words.

Co-mention-based features

Following the intuition that for a correct relation R=(object1,predicate,object2), object1 and object2 should occur in the same sentences of the scientific literature, we have tested several similarity measures that compute how often they occur in the same sentences. These co-mention similarity measures – Dice, Jaccard, Overlap, and Cosine [26] – are computed as defined in Table 3. These similarity measures are also computed while considering separately the title, the abstract, and the body of the documents, giving a total of 12 features.

Table 3 Co-mention similarity measures summarization

Context similarity-based features

Given a relation R=(object1,predicate,object2), the strength of the link associating the two objects can be estimated in a set of documents by evaluating the similarities of their context mentions in the text, following the intuition that two objects tend to be highly related if they share similar contexts. Hence, to evaluate the support of a given relation R that associates two objects given a set of documents, we define a context similarity matrix as follows:

Definition 2

A context similarity matrix \(\phantom {\dot {i}\!}M^{(o_{1},o_{2})}\) associated with a set of documents D is a matrix that reports the similarity between the context of two objects o1 and o2 such that each entry (i,j) estimates the similarity between the ith mention of the object o1 in the set D, and the jth occurrence of the object o2 in the set D.

Figure 4 shows the context similarity matrix for two objects, the gene “CFTR” and the disease “Cystic fibrosis (CF)”. This matrix indicates, for example, that the context of the first occurrence of the gene “CFTR” in the first returned document has a similarity of 0.16 with the context of the first occurrence of the disease CF in the same document. Similarly, the context of the first occurrence of the gene in that document has a similarity of 0.22 with the context of the first occurrence of the disease CF in the fourth returned document. Essentially, the concept–concept matrix captures the lexical similarity of the different occurrences of two objects in the documents returned by SaBRA. Once this matrix is built, we can calculate aggregate values based on the sum, standard deviation, minimum, maximum, arithmetic mean, geometric mean, harmonic mean, and coefficient of variation of all computed similarities. These aggregated values can be used as summaries of the link strength of the two objects.

Fig. 4

Toy example for building the context similarity matrix of the relational statement (CFTR, causes, CF) from the top 5 documents returned by SaBRA. Similarities are computed between the contexts of each occurrence of the two entities in the top documents. Aggregation values are then computed based on the obtained matrix to construct a feature vector

In the following, we first describe how we estimate the context distribution of a given object (word) in an article. Then, we describe different probabilistic-based metrics that we use to estimate the similarity between the contexts of the different occurrences of two objects.

Based on the method proposed by Wang and Zhai [27], who defined the context of a term based on a left and a right window size, we empirically found (results not shown) that the context of a word is best defined using sentence boundaries, as follows:

Definition 3

The context (C) of a document term w is the set of words that occur in the same sentence than w.

For example, in the sentence “Alice exchanged encrypted messages with Bob”, we say that the words “Alice”, “encrypted”, “messages”, “with”, and “Bob” are in the context C of the word “exchanged”.

Let C(w) denotes the set of words that are in the C context of w and count(a,C(w)) denotes the number of times that the word a occurs in the context C of w. Given a term w, the probability distribution of its context words using Dirichlet prior smoothing [28] is given by:

$$ \tilde{P}_{C}(a|w)=\frac{count(a,C(w))+\mu P(a|\theta)}{{\sum\limits_{i\in C(w)}count(i,C(w))}+\mu} $$

where P(a|θ) is the probability of the word a in the entire collection and μ is the Dirichlet prior parameter, which was empirically defined and set to 1500 in all of our experiments. Analogously, we define the double conditionalprobability distribution over the contexts of two words w1 and w2 as:

$$ \begin{aligned} \begin{array}{l} {}{\tilde{P}(c|w_{1},w_{2})=\frac{{count(c,C(w_{1}))+count(c,C(w_{2}))}+\mu P(c|\theta)}{{\sum\limits_{i\in C(w_{1})}\sum\limits_{j\in C(w_{2})}\left({count(i,C(w_{1}))+count(j,C(w_{2}))}\right)}+\mu}} \end{array} \end{aligned} $$

The similarity model is used to capture whether two objects of a relational statement are sharing the same context. The idea is that objects that occur in similar contexts are related to each another, and thus are highly correlated. In the following, we describe several similarity measures we used; these are fully described elsewhere [26].

Overlap:Overlap similarity is a similarity measure that measures the overlap between two sets and is defined as the size of the intersection divided by the smaller of the size of the two sets. In a probabilistic distributional case, it is defined as:

$$ {{\begin{aligned} {}{O(w_{1},w_{2})=\frac{{\sum\limits_{c\in C(w_{1})\cap C(w_{2})}\log\tilde{P}(c|w_{1},w_{2})}}{max\left({\sum\limits_{a\in C(w_{1})}\log\tilde{P}(a|w_{1})},{\sum\limits_{b\in C(w_{2})}\log\tilde{P}(b|w_{2})}\right)}} \end{aligned}}} $$

where \(\tilde {P}(a|w_{1})\) and \(\tilde {P}(b|w_{2})\) are defined in Eq. 2, and the joint probability \(\tilde {P}(c|w_{1},w_{2})\) is defined as in Eq. 3.

Matching: The matching similaritymeasure is defined as:

$$ M(w_{1},w_{2})={\sum\limits_{c\in C(w_{1})\cap C(w_{2})}\log\tilde{P}(c|w_{1},w_{2})} $$

Jaccard: The Jaccardsimilarity is a statistic metric used for comparing the similarity and diversity of sample sets. It is defined as the size of the intersection divided by the size of the union of the sample sets. In a probabilistic distributional case, it is defined as:

$$ J(w_{1},w_{2})=\frac{{\sum\limits_{c\in C(w_{1})\cap C(w_{2})}\log\tilde{P}(c|w_{1},w_{2})}}{{\sum\limits_{c\in C(w_{1})\cup C(w_{2})}\log\tilde{P}(c|w_{1},w_{2})}} $$

Dice: The Dice similarity measure is defined analogously to the harmonic mean between two sets. It considered as a semi-metric since it doesn’t satisfy the triangle inequality property. In a probabilistic distributional case, it is defined as follows:

$$ D(w_{1},w_{2})=\frac{2\times{\sum\limits_{c\in C(w_{1})\cap C(w_{2})}\log\tilde{P}(c|w_{1},w_{2})}}{{\sum\limits_{a\in C(w_{1})}\log\tilde{P}(a|w_{1})}+{\sum\limits_{b\in C(w_{2})}\log\tilde{P}(b|w_{2})}} $$

Cosine: The cosine similarity measure is defined as the inner product space that measures the cosine of the angle between vectors. In a probabilistic distributional case, it is defined as follows:

$$ {{\begin{aligned} {}Cos(w_{1},w_{2})=\frac{{\sum\limits_{c\in C(w_{1})\cap C(w_{2})}\log\tilde{P}(c|w_{1})}\log\tilde{P}(c|w_{2})}{\sqrt{{\sum\limits_{a\in C(w_{1})}\left[\log\tilde{P}(a|w_{1})\right]^{2}}}\times\sqrt{{\sum\limits_{b\in C(w_{2})}\left[\log\tilde{P}(b|w_{2})\right]^{2}}}} \end{aligned}}} $$

We apply these five similarity measures to build context similarity matrices, with each column constructed separately based on the title, the abstract, and the body of the returned documents. Once these matrices are built, we calculate for each matrix aggregation values based on the sum, standard deviation, minimum, maximum, arithmetic mean, geometric mean, harmonic mean, and coefficient of variation. In total, we have defined 120 context similarity-based features.


In summary, we have defined 300 word-level features for the inferred relation words, 12 co-mention-based features, and 120 context similarity-based features. Therefore, for each relational statement we have a total of 432 feature values, which can be represented as a feature vector xm=[xm1,xm2,…,xm432].

Supervised learning algorithm

Given as input a set of features for each relation to assess, our goal is to combine these inputs to produce a value indicating whether this relation is correct or incorrect given the scientific literature. To accomplish this, we use SVMs [29], one of the most widely-used and effective classification algorithms.

Each relation Rm is represented by its vector of 432 features xm=[xm1,xm2,…,xm432] and its associated label ym{correct,incorrect}. We used the SVM implementation available in the LibSVM package [30]. Both Linear and RBF kernels were considered in our experiments. The regularization parameter C (the trade-off between training error and margin), and the gamma parameter of the RBF kernel are selected from a search within the discrete sets {10−5,10−3,…,1013,1015}, and {10−15,10−13,…,101,103}, respectively. Each algorithm is assessed using a nested cross validation approach, which effectively uses a series of 10 train–test set splits. The inner loop is responsible for model selection and hyperparameter tuning (similar to a validation set), while the outer loop is for error estimation (test set), thus, reducing the bias.

In the inner loop, the score is approximately maximized by fitting a model that selects hyper-parameters using 10-fold cross-validation on each training set. In the outer loop, efficiency scores are estimated by averaging test set scores over the 10 dataset splits. Although the differences were not substantial, initial experiments with the best RBF kernel parameters performed slightly better than the best linear kernel parameters for the majority of the validation experiments. Unless otherwise noted, all presented results were obtained using an RBF kernel, with C and gamma set to the values that provide the best accuracy.

Experimental data

We first describe the collection of documents we have used for the evaluation, then describe the two types of relations we have considered.

Literature: We used the PubMed Central Open Access collectionFootnote 6 (OA), which is a free full-text archive of biomedical and life sciences journal literature at the US National Institutes of Health’s National Library of Medicine. The release of PMC OA we used contains approximately 1.13 million articles, which are provided in an XML format with specific fields corresponding to each section or subsection in the article. We indexed the collection based on genes/proteins and diseases that were detected in the literature while focusing on human species. To identify genes or proteins in the documents we used GNormPlus [31]. (Note that the namespace for genes and proteins overlaps significantly and this tool does not distinguish between genes or proteins.) GNormPlus has been reported to have precision and recall of 87.1% and 86.4%, respectively, on the BioCreative II GN test set. To identify disease mentions in the text, we used DNorm [32], a tool reported to have precision and recall of 80.3% and 76.3%, respectively, on the subset of the NCBI disease corpus. The collection of documents is indexed at a concept level rather than on a word level, in that synonyms, short names, and long names of the same gene or disease are all mapped and indexed as the same concept. Also, each component of each article (title, abstract, body) is indexed separately, so that different sections can be used and queried separately to compute the features [33].Gene-disease relations: The first type of relation that we used to evaluate BARC is etiology of disease, that is, the gene-causes-disease relation. To collect correct gene–disease relations (positive examples), we used a curated dataset from Genetics Home Reference provided by the Jensen Lab [34]Footnote 7. Note that we kept only relations for which GNormPlus and DNorm identified at least a single gene and disease respectively. To build a test set of incorrect relations (negative examples), we used the Comparative Toxicogenomics Database (CTD), which contains both curated and inferred gene–disease associations [20].

The process for generating negative examples was as follows: (i) We determined the set of documents from which the CTD dataset has been built, using all PubMed article identifiers referenced in the database for any relation. (ii) We automatically extracted all sentences in which a gene and a disease are co-mentioned (co-occur) that appear in the set of documents, and identified the unique set of gene–disease pairs across these sentences. (iii) We removed all gene–disease pairs that are known to be valid, due to being in the curated CTD dataset. (iv) We manually reviewed the remaining gene–disease pairs, and removed all pairs for which evidence could be identified that suggested a valid (correct) gene–disease relation (10% of the pairs were removed at this step by reviewing about 5–10 documents for each relation). The remaining pairs are our set of negative examples. We consider this data set to consist of reliably incorrect relations (reliable negatives), based on the assumption that each article that is completely curated, that is, that any relevant gene–disease relationship in the article is identified. This is consistent with the article-level curation that is performed by the CTD biocurators [20].

Protein-protein interactions: The second kind of relation we used to evaluate BARC is protein–protein interactions (PPIs). We used the dataset provided by BioGRID as the set of correct relations [35].Footnote 8 We kept only associations for which the curated documents are in our collection. To build a test set of incorrect relational statements, we proceeded similarly to the previous case, again under the assumption that all documents are exhaustively curated; if the document is in the collection, all relevant relations should have been identified.

We describe our dataset in Table 4. For example, articles cite 6.15 genes on average; the article PMC100320Footnote 9 cites 2040 genes. A gene is cited on average 24.6 times, while the NAT2Footnote 10 is the most cited gene. GNormPlus and DNorm identified respectively roughly 54M genes and 55M diseases in the collection.

Finally, in the experimental evaluation, we consider a total of 1991 gene–disease relations, among which 989 are correct and 1002 are incorrect. On average each mention is in 141.9 documents, with a minimum of 1 and a maximum of 12,296. Similarly, we consider a total of 4,657 protein–protein interactions among which 1758 are correct and 2899 are incorrect. Hence, our test set has reasonable balance.


Our experiments address the following questions, in the context of the task of classifying whether or not a given relational assertion is supported by the literature:

  1. 1

    How well does SaBRA perform the task of building a relevant set for feature extraction, compared to other retrieval methods?

  2. 2

    How well does SaBRA perform on relations with different document support values for the two objects involved in these relations?

  3. 3

    How does BARC compare with other approaches to the same task?

Evaluation of SaBRA

Given that SaBRA is designed to retrieve documents for a specific task of classification, standard evaluation approaches and metrics of information retrieval are not applicable. Therefore, we chose to evaluate the performance of SaBRA by examining the general performance of the classification task, that is, the performance of BARC. As baselines, we compared SaBRA with two well-known scoring functions: TF-IDF and Okapi BM25. Note that we also use named entities for the retrieval step and that we use these two functions for ranking only.Footnote 11 Specifically, TF-IDF and BM25 are applied in place of lines 6-13 in Algorithm 14, to order the documents previously retrieved on lines 3-5. The performance is assessed using conventional metrics used to evaluate a classifier, namely: precision, recall, accuracy, Receiver Operating Characteristic curve (ROC curve), and Area Under the ROC curve (ROC AUC).

The results of the comparison are shown in Figs. 5 and 6 for gene–disease relations and protein–protein interactions respectively. We also show results obtained for values of k{1,2,3,5,10,15,20,25,30}, which is the number of top documents returned by the retrieval algorithms. From the results, we make the following observations.

Fig. 5

Comparison of SaBRA with TF-IDF and BM25 scoring functions using gene-disease relations. a Precision for correct statements. b Recall for correct statements. c Classification Accuracy. d ROC AUC. e ROC K =1. f ROC K =2. g ROC K =3. h ROC K =5. i ROC K =10. j ROC K =15. k ROC K =20. l ROC K =25. m ROC K =30

Fig. 6

Comparison of SaBRA with TF-IDF and BM25 scoring functions using protein-protein interactions. a Precision for correct statements. b Recall for correct statements. c Classification Accuracy. d ROC AUC. e ROC K =1. f ROC K =2. g ROC K =3. h ROC K =5. i ROC K =10. j ROC K =15. k ROC K =20. l ROC K =25. m ROC K =30

In general, the method works well. BARC achieves an accuracy of roughly 89% and 79%, respectively, for the gene–disease relations and protein–protein interactions. The higher the value of k, the higher the performance of the classification. This is almost certainly due to the fact that the higher the number of aggregated documents, the more likely it is that the features are informative, and thus, the higher the performance of the classification. However, we note that performance is more or less stable above k=10 for both gene–disease relations and protein–protein interactions. Considering more documents in both cases results in only marginal improvement.

While the performance obtained when varying k on the gene–disease relations is smooth (the performance keeps increasing as k increases), the performance while varying k on the protein–protein interactions is noisy. For example, for k=3 SaBRA achieved 65% recall, but for k=5 the recall dropped to 56%, which means the two documents added are probably irrelevant for building a relevant set of documents. Similar observations can also be made for the two baselines. For almost all values of k, SaBRA outperforms the two retrieval baselines BM25 and TF-IDF. While SaBRA clearly outperforms BM25 (roughly 13% for recall, 6% for accuracy, 5% ROC AUC for gene–disease relations), the improvement over TF-IDF is lower. In the next section, we explore how SaBRA performs on different statements with respect to the two retrieval algorithms.

Overall, the performance obtained on the gene–disease relations is higher than that obtained for protein–protein interactions. This is probably because genes and diseases that are related tend to be more often associated in the literature than are proteins that interact; indeed, gene–disease relations attract more attention from the research community. Therefore, there is more sparsity in the protein–protein interactions test set. This is also reported in Table 4, where on average each gene–disease relation has a support of 141.9, whereas each protein–protein interaction relation has a support of 14.1.

Performance on different relations

Relational statements may be analyzed using the support criteria to identify the most important or frequent relationships. We define the support as a measurement of how frequently the relations appear in the same documents in the literature. Clearly, correct relations with low support values are of weaker association evidence than correct relations with high support values. Analogously, incorrect relations with high support values may be of stronger association evidence than incorrect relations with low support values. Therefore, we perform an evaluation analysis based on relations with different document support values.

In order to evaluate BARC in general and SaBRA in particular on relations with document support values, we first group all the relations based on the document support values in the dataset, and then evaluate the accuracy of different relation groups. Results comparing SaBRA against the other retrieval methods are shown in Fig. 7. For gene–disease relations, we build eight classes: “1”, “2 − 5”, “6 − 14”, “15 − 29”, “30 − 60”, “61 − 125”, “126 − 335”, and “> 335”, denoting the document support values for each group. As for the protein–protein interactions, relations are grouped in 6 classes: : “1”, “2 − 3”, “4 − 8”, “9 − 30”, “31 − 100”, and “> 100”.

Fig. 7

Performance comparison of SaBRA on different relations with different document support values for k=30. a Performance comparison for different document support values on gene-disease relations. b Distribution of gene-disease relations. c Performance comparison for different document support values on protein-protein interactions. d Distribution of protein-protein interactions

Figure 7b and d summarize the distributions of, respectively, the gene–disease relations and the protein–protein interactions according to the groups defined. For example, in Fig. 7b, there are a total of 135 gene–disease relations evaluated in for which the document support values equal to 1. The performance is evaluated in terms of accuracy in Fig. 7a and c. SaBRA generally performs better than the other methods.

The conclusions drawn are different for the two relational statements evaluated. For gene–disease relations with low document support values (“1”), SaBRA performs much better than TF-IDF and BM25, and increases the performance with roughly 10% and 18% respectively. As the document support values increase, the performances of all the algorithms increase and converge, but SaBRA still generates better predictions than the other methods at all levels.

For protein–protein relations with high document support values (“>100”), SaBRA performs much better than TF-IDF and BM25, and increases the performance with roughly 12% and 19% respectively. However, as the document support values decrease, the performance of SaBRA is consistent but the performances of TF-IDF and BM25 increase. TF-IDF is even doing slightly better than SaBRA for relations with document support values in the range “1-3”, yielding an improvement of roughly 1%.

Classification performance

In the previous sections we focused on the evaluation of SaBRA, the ranking algorithm used in BARC. Here, we evaluate BARC itself with respect to straightforward baselines (noting that there is no prior published method for our task). For the baselines, we used both an SVM classifier as well as the C4.5 decision tree algorithm [36]. We have chosen to use a decision tree for the baselines as it can be linearized into decision rules, which may reflect the decisions taken manually by a biocurator who wishes to assess the correctness of relations. We argue that a decision-tree algorithm represents the closest algorithmic analog to a human biocurator who is assessing relations. We used different co-mention-based features to train several decision trees as follows:

  • Baseline 1: Trained using document support values. The idea is that the higher the document support value, the higher the probability that the relationship is correct.

  • Baseline 2: Trained using mutual information (MI) values based on co-mention of the two objects involved in a relation I(o1;o2). We recall that MI is a measure of the mutual dependence between the two variables.

  • Baseline 3: Trained using document support values computed for each document field (three features are used). This baseline can be seen as a more elaborated version of Baseline 1.

  • Baseline 4: Trained using mutual information (MI) values computed for each document field (three features are used). This baseline can be seen as a more elaborated version of Baseline 2.

  • WordEmb: This baseline method relies on word embeddings,Footnote 12 which may effectively allow consideration of indirect relations between pairs of objects. We developed several features extracted from the embeddings, including vector dot products and element-wise multiplication.

Results are shown in Fig. 8a and b for the gene–disease relations and the protein–protein interactions, respectively. Comparing the baselines, we first observe that the best results are those based on SVM as we may expect. This is because SVM tries to maximize the margin between the closest support vectors while Decision Trees maximize the information gain. Thus, SVM finds a solution which separates the two categories as far as possible while Decision Trees do not have this capability. BARC clearly outperforms the baselines on the two test sets. We also note that for the two test sets, the performance of BARC is stable compared to the other baselines; for example, Baseline 4 has a high recall value on gene–disease relations and thus is ranked second on that test set, but a low recall value on the protein–protein interactions and thus is ranked fourth on that test set. Finally, we observe that the word-embedding baseline is the best performing baseline on the gene-disease relations, and nearly as effective as BARC (which achieves only 3.5% improvement in F-Measure over the word embedding baseline). However, the word-embedding baseline is much less effective than BARC on the protein-protein interaction dataset. After a thorough investigation, we find that, compared to all baselines over the two datasets, the word-embedding approach has stable performance between the two tasks. However, BARC achieves higher performance on the protein–protein interactions dataset than on the gene–disease interactions dataset. We explain this primarily by the fact that the tool that we used to identify genes and proteins in the literature has a higher accuracy than the tool we used to identify diseases. Therefore, BARC could more accurately capture the context of the protein–protein interactions to correctly classify the corresponding relations.

Fig. 8

Performance comparison of BARC for k=30. DT: Decision Tree-based classification. a Performance comparison on gene–disease relations. b Performance comparison on protein–protein interactions


In this section, we first provides a discussion on the informativeness of features and then we discuss the limitations of our method.

Features analysis

To explore the relationship between features and the relation consistency labels, we undertook a feature analysis. Specifically, we performed a mutual information analysis at the level of individual features and feature ablation analysis at the level of feature category.

Mutual information analysis

A general method for measuring the amount of information that a feature xk provides with respect to predicting a class label y (“correct” or “incorrect”) is to calculate its mutual information (MI) I(xk,y). In Table 5, we present the list of 10 top-ranked features, and in Fig. 9, we show a complete overview of MI values obtained for each feature using a heatmap.

Fig. 9

Feature analysis using MI. The higher the density color, the higher the MI value. a Gene-Disease relations. b Protein-Protein interactions

Table 5 Ranking of the most important features using MI

This analysis led us to make the following observations. On both relations, the top features are the inferred relation words. Specifically, as we may expect, the words “mutation” and “interact” are the most discriminative for respectively gene–disease relations and protein–protein interactions. However, based on Fig. 9, all feature kinds are informative, as well as all document fields. Features computed on the body of documents are the most informative, particularly for inferred relation word and co-mention based features. For context-based features on the gene–disease relations, the titles of documents seem to be more informative than the other fields. This indicates that correct gene–diseases relations tend to be mentioned in the title of articles.

Given the large number of features and similarity metrics we have defined, we show in Table 6 the correlation between similar features for the different types of features using PCA. This table shows the most related and independent features. Also, this analysis shows which feature inside each feature group is most important. Based on the results we obtained, we make the following observations: correlated features come usually from similar fields of documents; all documents fields are useful for extraction of informative features; similar aggregation functions generate correlated features.

Table 6 Top correlated features within each group of features obtained using PCA

Feature ablation analysis

A feature ablation study typically refers to removing some “feature group” of the model, and observing how that affects performance. Hence, we propose to study the impact of each feature group individually on the global performance. The results obtained are shown in Fig. 10 for both gene–disease relations and protein–protein interactions.

Fig. 10

Feature ablation analysis (k=30). a Performance on gene–disease relations. b Performance on protein–protein interactions

We make the following observations: For gene–disease relations, the best feature groups are in the following order: inferred relation word features followed by context features and then by co-mention features. For the protein–protein interactions, the best feature groups are in the following order: inferred relation word features followed by co-mention features and then by context features. On the protein–protein interactions, all features lead to similar performance, yielding only marginal improvements on each other. The combination of the three feature groups on the gene–disease relations is producing marginal improvements. However, their combination slightly improves the performance on the protein–protein interactions, boosting precision from 76% for inferred relation word features to 84% (an improvement of roughly 10.5%).


There are limitations in our approach. Currently, BARC incorrectly identifies negative sentences, expressing that two objects do not interact in a given relation, as positive instances of their interaction. For example, given a document that contains a sentence such as: “Gene X does not affect the expression in Syndrome Y”, may count as a support of the relation (geneX, affect, SyndromeY). However, given the positivity bias of research publications, we expect such negative statements to be outweighed by positive statements of true interactions. The issue could be addressed by explicit treatment of negation, either through a naïve approach of removing sentences containing negation key terms, or through analysis of sentence structure to identify negated relations, for instance as done in the BioNLP Shared Task [37].

Second, BARC relies on the capability and accuracy of named-entity-recognition tools to extract object mentions from the literature. Even though the tools we have used to extract gene and disease mentions from the literature have reasonable accuracy, we assumed in this work that they are highly reliable. Thus, we have not considered the impact of their errors on the results that we have reported.

Finally, BARC also relies on the fact that valid and correct relationships are expected to occur in the same documents and sentences. Indeed, if a given relationship between two entities is supported by the literature, they should be discussed in individual documents, and moreover in the same sentences, to be correctly classified by BARC. Conversely, a valid relationship that is not directly stated in the literature will not be correctly classified by BARC. This could be addressed by enhancing BARC with external sources of knowledge.

Related work

There is a substantial body of research related to named entity recognition, relation extraction, and the use of structured or unstructured knowledge for checking statements and answering questions. Hence, we review below the major works related to these aspects.

Named entity recognition (NER)

Recognition of named entities and concepts in text, such as genes and diseases, is the basis for most biomedical applications of text mining [38]. NER is sometimes divided into two subtasks: recognition, which consists of identifying words of interest, and normalization, which consists of mapping the identified entities to the correct entries in a dictionary. However, as noted by Pletscher-Frankild et al. [34], because recognition without normalization has limited practical use the normalization step is now often implicitly considered part of the NER task.

In brief, the main issues with NER in the biological literature occur because of the poor standardization of names and the fact that a name of an entity may have other meanings [39]. To recognize names in text, many systems make use of rules that look at features of names themselves, such as capitalization, word endings and the presence of numbers, as well as contextual information from nearby words. In early methods, rules were hand-crafted [40], whereas newer methods make use of machine learning and deep learning techniques [41, 42], relying on the availability of manually annotated training datasets.

Dictionary-based methods instead rely on matching a dictionary of names against text. For this purpose the quality of the dictionary is obviously very important; the best performing methods for NER according to blind assessments rely on carefully curated dictionaries to eliminate synonyms that give rise to many false positives [43, 44]. Moreover, dictionary-based methods have the crucial advantage of being able to normalize names. Whether or not use is made of machine learning, a high-quality, comprehensive dictionary of gene and disease names is a prerequisite for mining disease–gene associations from the biomedical literature.

Relation extraction

Relation extraction is the task of extracting semantic relationships between named entities mentioned in a text. Relation extraction methods are usually divided into two categories [45, 46], namely: feature-based and kernel-based supervised learning approaches. In feature-based methods, for each relation instance in the labelled data, a set of features is generated and a classifier is then trained to classify any new relation instance [4749]. On the other hand, kernel based methods use kernel functions to compute similarities between representations of two relation instances and SVM is employed for classification. Two major kernel approaches are used: bag-of-features kernels [50, 51] and tree or graph kernels [5254, 5456].

With the rise of deep learning, several neural network models have been used for relation extraction while achieving obtained state-of-the-art performance. Two major neural architectures were used including convolutional neural networks (CNNs) [5763] and recurrent neural networks (RNNs) [6467]. Combinations of these two architectures have also been proposed [6870].

Methods for assessing statements

Identifying correct and incorrect statements is a problem that has been widely explored in the literature using various techniques ranging from pure information retrieval to crowdsourcing, and used in many applications such as fact-checking in journalism and the support of biomedical evidence from the literature. We review below the major work related to our paper.


Several approaches have been recently proposed to check the truthfulness of facts, particularly in the context of journalism [71]. Most of the methods proposed assume the availability of structured knowledge modeled as a graph, which is then used to check the consistency of facts. Hence, recent works addressed this problem as a graph search problem [72, 73], a link prediction problem [74], or a classification and ranking problem [75].

However, the aforementioned methods rely on the availability of a knowledge graph, which limits and reduces the scope and the impact of any method as: it requires a specific knowledge graph for each domain (eventually sub-domain), and may fail in real-time assessment of facts, as it requires continuous update of the knowledge graph, a task generally done by domain-specialists. BARC may overcome these two limitations as it uses a standard index, which can easily be updated to address new facts.

Supporting biomedical evidence

In the context of biocuration, the information retrieval task that consists of finding relevant articles for the curation of a biological database is called triage [7680]. Triage can be seen as a semi-automated method for assessing biological statements; it assists curators in the selection of relevant articles, which then must be manually reviewed to decide their correctness. As mentioned in the Introduction, this triage process is time-consuming and expensive [4, 5]; curation of a single protein may take up to a week and requires considerable human investment both in terms of knowledge and effort [6]. Rather, BARC is a fully automated method that directly helps biocurators to assess biological database assertions using the scientific literature.

Also, in the biomedical context, Light et al. [81] used a handcrafted list of cues to identify speculative sentences in MEDLINE abstract by looking for specific keywords which imply speculative content. However, it is unclear how this method generalizes to relations that are mentioned in both speculative and non-speculative sentences. Leach et al. [82] proposed a knowledge-based system that combines reading, reasoning, and reporting methods to facilitate analysis of experimental data, which was then applied to the analysis of a large-scale gene expression array data sets relevant to craniofacial development. This method combines and integrates multiple sources of data into a knowledge network through a reading and a reasoning component; as it requires complex mappings to identify and link entities in order to get a consistent knowledge graph, it may fail to scale to large datasets. Zerva et al. [83] proposed the use of uncertainty as an additional measure of confidence for interactions in biomedical pathway network supported by evidence from literature for model curation. The method is based on using a hybrid approach that combines rule induction and machine learning. This method focuses on biomedical pathways and uses features specifically designed to detect uncertain interactions. However, its generalisation for assessment other statements is unclear and is not discussed in the paper. Several other papers [84, 85] have focused on extracting relations from text using distant supervision multi-instance learning to reduce the amount of manual effort for labeling. Such work demonstrates that the approach can be successfully used to extract relations from literature about a biological process with little or no manually annotated corpus data. This method might be complementary to BARC; it may allow the extraction of new relevant features that characterize the relationships between entities. Note that BARC is capable of overcoming all the drawbacks mentioned for these approaches, as it does not require any data integration or complex mappings and it has been designed in such a way to assess multiple types of statements.

Crowdsourcing-based methods

Crowdsourcing has attracted interest in the bioinformatics domain for data annotation [86]. It has been successfully applied in the biomedical and clinical domains [87]. This research has demonstrated that crowdsourcing is an inexpensive, fast, and practical approach for collecting high quality annotations for different BioIE tasks [88], including NER in clinical trial documents [89], disease mention annotation in PUBMED literature [90], relation extraction between clinical problems and medications [91], etc. Different techniques have been explored to improve the quality and effectiveness of crowdsourcing, including probabilistic reasoning [92] to make sensible decisions on annotation candidates and gamification strategies [93] to motivate the continuous involvement of the expert crowd. More recently, a method called CrowdTruth [94] was proposed for collecting medical ground truth through crowdsourcing, based on the observation that disagreement analysis on crowd annotations can compensate lack of medical expertise of the crowd. Experiments with the use of CrowdTruth for a medical relation extraction task show that the crowd performs just as well as medical experts in terms of quality and efficacy of annotation, and also indicate that at least 10 workers per sentence are needed to get the highest quality annotation for this task. Crowdsourcing holds promise for biocuration tasks as well and could be combined with prioritisation methods such as BARC provides.

Information retrieval-based methods

In the context of information retrieval, despite the development of sophisticated techniques for helping users to express their needs, many queries still remain unanswered [95]. Hence, to tackle these issues, other types of question-answering (QA) systems have emerged to allow people to help each other to answer questions [96]. Community QA systems provide a means for answering several types of questions such as recommendation, opinion seeking, factual knowledge, or problem solving [96]. (Therefore, QA systems can help to answer specific and contextualised questions, and hence, could potentially be used by biocurators for seeking answers to questions like those given as examples in “Problem definition” section.

A challenge facing such systems is in the response time as well as the quality of the answers [95, 9799]. However, the time factor is critical in the context of biocuration as there is a huge quantity of information to be curated. Such waiting times to answer questions probably disqualify this body of work for their usage in biocuration.

These methods that use unstructured knowledge (that is, the literature) for fact-checking and query answering address the problem as a pure information retrieval problem. In other words, these methods rank documents (or sentences) relevant to a given information need, and it is up to the user to read and search for a support to a given assertion or question. In contrast, BARC allows spotting of potentially incorrect assertions, and presents them to the user with, in our experiments, a high classification accuracy.


We have described BARC, a tool that aims to help biocurators in checking the correctness of biological relations using the scientific literature. Specifically, given a new biological assertion represented as a relation, BARC first retrieves a list of documents that may be used to check the correctness of that relation. This retrieval step is done using a set-based retrieval algorithm (SaBRA). This list of documents is aggregated in order to compute features for the relation as a whole, which are used for a prediction task.

We evaluated BARC and retrieval algorithm SaBRA using publicly available datasets including the PubMed Central collection and two types of relational assertions, gene–disease relations, and protein–protein interactions. The results obtained showed that BARC substantially outperforms the best baselines, with an improvement of F-measure of 3.5% and 13%, respectively, on gene-disease relations and protein-protein interactions. We have additionally carried out a feature analysis that showed that all feature types are informative, as are all fields of the documents. A limitation of this work is that it relies on the accuracy of the GNormPlus [31] and DNorm [32] entity recognition tools; these are automated tools and hence subject to error. We note further that in this paper BARC has been evaluated on only two kinds of relations; we leave the analysis of its generalization to future work, such as drug-disease or drug-drug interactions. However, the results show that the methods are effective enough to be used in practice, and we believe they can provide a valuable tool for supporting biocurators.


  1. 1.

  2. 2.

  3. 3.

  4. 4.

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    Atopy refers to the genetic tendency to develop allergic diseases such as allergic rhinitis, asthma and atopic dermatitis (eczema).

  6. 6., downloaded October 2015.

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  8. 8. 3.4.150)

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    Table 4 Dataset statistics
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  11. 11.

    We used the Lucene implementation of TF-IDF and Okapi BM25,

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    We used word vectors induced from PMC by Pyysalo et al. [100]:



Biocuration tool for assessment of relation consistency


Comparative toxicogenomics database


False positive


Protein-protein interaction


Radial basis function


Receiver operating characteristic


Set-based retrieval algorithm


Support vector machine


Term frequency-inverse document frequency


True positive


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Experiments presented in this paper were carried out using the NECTAR Research Cloud platform, supported by a scientific interest group hosted by several Australian Universities (see We would like to further thank anonymous reviewers for their insights and advice about this manuscript.


The project receives funding from the Australian Research Council through a Discovery Project grant, DP150101550. The funding agency played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

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All authors contributed to the conceptualisation of BARC and its approach. MRB designed and implemented the new algorithm SaBRA. MRB and KV planned the experiments. All authors contributed to interpretation and analysis of results. All authors were involved with writing, and approved the final manuscript.

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Correspondence to Mohamed Reda Bouadjenek.

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Availability of data and materials

All data and material used in this paper are from public datasets. PubMed Central Open Access collection is available at:; Gene-Disease relations extracted from Comparative Toxicogenomics Database (CTD) are available at:; and protein-protein interactions extracted from BioGRID are available at:

This work has been primarily completed while the author was a researcher at The University of Melbourne.

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Bouadjenek, M., Zobel, J. & Verspoor, K. Automated assessment of biological database assertions using the scientific literature. BMC Bioinformatics 20, 216 (2019).

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  • Data Analysis
  • Data Quality
  • Biological Databases
  • Data Cleansing