Abstract

BackgroundDue to the importance of identifying relations between chemicals and diseases for new drug discovery and improving chemical safety, there has been a growing interest in developing automatic relation extraction systems for capturing these relations from the rich and rapid-growing biomedical literature. In this work we aim to build on current advances in named entity recognition and a recent BioCreative effort to further improve the state of the art in biomedical relation extraction, in particular for the chemical-induced disease (CID) relations.ResultsWe propose a rich-feature approach with Support Vector Machine to aid in the extraction of CIDs from PubMed articles. Our feature vector includes novel statistical features, linguistic knowledge, and domain resources. We also incorporate the output of a rule-based system as features, thus combining the advantages of rule- and machine learning-based systems. Furthermore, we augment our approach with automatically generated labeled text from an existing knowledge base to improve performance without additional cost for corpus construction. To evaluate our system, we perform experiments on the human-annotated BioCreative V benchmarking dataset and compare with previous results. When trained using only BioCreative V training and development sets, our system achieves an F-score of 57.51 %, which already compares favorably to previous methods. Our system performance was further improved to 61.01 % in F-score when augmented with additional automatically generated weakly labeled data.ConclusionsOur text-mining approach demonstrates state-of-the-art performance in disease-chemical relation extraction. More importantly, this work exemplifies the use of (freely available) curated document-level annotations in existing biomedical databases, which are largely overlooked in text-mining system development.

Highlights

  • Due to the importance of identifying relations between chemicals and diseases for new drug discov‐ ery and improving chemical safety, there has been a growing interest in developing automatic relation extraction systems for capturing these relations from the rich and rapid-growing biomedical literature

  • Different from previous relation extraction tasks such as protein–protein interaction, disease-gene association, and miRNA-gene interaction [23, 25, 28,29,30,31,32, 44], the BC5 task requires the output of extracted relations with entities normalized to a controlled vocabulary (the National Library of Medicine’s Medical Subject Headings (MeSH) identifiers were used)

  • Not all pairs of chemicals and diseases are involved in a chemical-induced disease (CID) relation

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Summary

Introduction

Due to the importance of identifying relations between chemicals and diseases for new drug discov‐ ery and improving chemical safety, there has been a growing interest in developing automatic relation extraction systems for capturing these relations from the rich and rapid-growing biomedical literature. In this work we aim to build on current advances in named entity recognition and a recent BioCreative effort to further improve the state of the art in biomedical relation extraction, in particular for the chemical-induced disease (CID) relations. To reduce risk and the development time, there has been considerable interest in identifying chemical-induced disease (CID) relations between existing chemicals and disease phenotypes by computational methods. Such efforts are important for improving chemical safety and for informing potential relationships between chemicals and pathologies [53]. There is no relation between “midazolam” and “death” in Fig. 1 because the task guidelines consider “death” to be too general

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