Datasets for generic relation extraction

A vast amount of usable electronic data is in the form of unstructured text. The relation extraction task aims to identify useful information in text (e.g. PersonW works for OrganisationX, GeneY encodes ProteinZ) and recode it in a format such as a relational database or RDF triplestore that can be more effectively used for querying and automated reasoning. A number of resources have been developed for training and evaluating automatic systems for relation extraction in different domains. However, comparative evaluation is impeded by the fact that these corpora use different markup formats and notions of what constitutes a relation. We describe the preparation of corpora for comparative evaluation of relation extraction across domains based on the publicly available ACE 2004, ACE 2005 and BioInfer data sets. We present a common document type using token standoff and including detailed linguistic markup, while maintaining all information in the original annotation. The subsequent reannotation process normalises the two data sets so that they comply with a notion of relation that is intuitive, simple and informed by the semantic web. For the ACE data, we describe an automatic process that automatically converts many relations involving nested, nominal entity mentions to relations involving non-nested, named or pronominal entity mentions. For example, the first entity is mapped from 'one' to 'Amidu Berry' in the membership relation described in 'Amidu Berry, one half of PBS'. Moreover, we describe a comparably reannotated version of the BioInfer corpus that flattens nested relations, maps part-whole to part-part relations and maps n-ary to binary relations. Finally, we summarise experiments that compare approaches to generic relation extraction, a knowledge discovery task that uses minimally supervised techniques to achieve maximally portable extractors. These experiments illustrate the utility of the corpora.39 page(s

One for All: Neural Joint Modeling of Entities and Events

The previous work for event extraction has mainly focused on the predictions for event triggers and argument roles, treating entity mentions as being provided by human annotators. This is unrealistic as entity mentions are usually predicted by some existing toolkits whose errors might be propagated to the event trigger and argument role recognition. Few of the recent work has addressed this problem by jointly predicting entity mentions, event triggers and arguments. However, such work is limited to using discrete engineering features to represent contextual information for the individual tasks and their interactions. In this work, we propose a novel model to jointly perform predictions for entity mentions, event triggers and arguments based on the shared hidden representations from deep learning. The experiments demonstrate the benefits of the proposed method, leading to the state-of-the-art performance for event extraction.Comment: Accepted at The Thirty-Third AAAI Conference on Artificial Intelligence (AAAI-19) (Honolulu, Hawaii, USA

NEREL-BIO: A Dataset of Biomedical Abstracts Annotated with Nested Named Entities

This paper describes NEREL-BIO -- an annotation scheme and corpus of PubMed abstracts in Russian and smaller number of abstracts in English. NEREL-BIO extends the general domain dataset NEREL by introducing domain-specific entity types. NEREL-BIO annotation scheme covers both general and biomedical domains making it suitable for domain transfer experiments. NEREL-BIO provides annotation for nested named entities as an extension of the scheme employed for NEREL. Nested named entities may cross entity boundaries to connect to shorter entities nested within longer entities, making them harder to detect. NEREL-BIO contains annotations for 700+ Russian and 100+ English abstracts. All English PubMed annotations have corresponding Russian counterparts. Thus, NEREL-BIO comprises the following specific features: annotation of nested named entities, it can be used as a benchmark for cross-domain (NEREL -> NEREL-BIO) and cross-language (English -> Russian) transfer. We experiment with both transformer-based sequence models and machine reading comprehension (MRC) models and report their results. The dataset is freely available at https://github.com/nerel-ds/NEREL-BIO.Comment: Submitted to Bioinformatics (Publisher: Oxford University Press

Mining clinical relationships from patient narratives

Background The Clinical E-Science Framework (CLEF) project has built a system to extract clinically significant information from the textual component of medical records in order to support clinical research, evidence-based healthcare and genotype-meets-phenotype informatics. One part of this system is the identification of relationships between clinically important entities in the text. Typical approaches to relationship extraction in this domain have used full parses, domain-specific grammars, and large knowledge bases encoding domain knowledge. In other areas of biomedical NLP, statistical machine learning (ML) approaches are now routinely applied to relationship extraction. We report on the novel application of these statistical techniques to the extraction of clinical relationships. Results We have designed and implemented an ML-based system for relation extraction, using support vector machines, and trained and tested it on a corpus of oncology narratives hand-annotated with clinically important relationships. Over a class of seven relation types, the system achieves an average F1 score of 72%, only slightly behind an indicative measure of human inter annotator agreement on the same task. We investigate the effectiveness of different features for this task, how extraction performance varies between inter- and intra-sentential relationships, and examine the amount of training data needed to learn various relationships. Conclusion We have shown that it is possible to extract important clinical relationships from text, using supervised statistical ML techniques, at levels of accuracy approaching those of human annotators. Given the importance of relation extraction as an enabling technology for text mining and given also the ready adaptability of systems based on our supervised learning approach to other clinical relationship extraction tasks, this result has significance for clinical text mining more generally, though further work to confirm our encouraging results should be carried out on a larger sample of narratives and relationship types

From POS tagging to dependency parsing for biomedical event extraction

Background: Given the importance of relation or event extraction from biomedical research publications to support knowledge capture and synthesis, and the strong dependency of approaches to this information extraction task on syntactic information, it is valuable to understand which approaches to syntactic processing of biomedical text have the highest performance. Results: We perform an empirical study comparing state-of-the-art traditional feature-based and neural network-based models for two core natural language processing tasks of part-of-speech (POS) tagging and dependency parsing on two benchmark biomedical corpora, GENIA and CRAFT. To the best of our knowledge, there is no recent work making such comparisons in the biomedical context; specifically no detailed analysis of neural models on this data is available. Experimental results show that in general, the neural models outperform the feature-based models on two benchmark biomedical corpora GENIA and CRAFT. We also perform a task-oriented evaluation to investigate the influences of these models in a downstream application on biomedical event extraction, and show that better intrinsic parsing performance does not always imply better extrinsic event extraction performance. Conclusion: We have presented a detailed empirical study comparing traditional feature-based and neural network-based models for POS tagging and dependency parsing in the biomedical context, and also investigated the influence of parser selection for a biomedical event extraction downstream task. Availability of data and material: We make the retrained models available at https://github.com/datquocnguyen/BioPosDepComment: Accepted for publication in BMC Bioinformatic

On Generative Models and Joint Architectures for Document-level Relation Extraction

Biomedical text is being generated at a high rate in scientific literature publications and electronic health records. Within these documents lies a wealth of potentially useful information in biomedicine. Relation extraction (RE), the process of automating the identification of structured relationships between entities within text, represents a highly sought-after goal in biomedical informatics, offering the potential to unlock deeper insights and connections from this vast corpus of data. In this dissertation, we tackle this problem with a variety of approaches. We review the recent history of the field of document-level RE. Several themes emerge. First, graph neural networks dominate the methods for constructing entity and relation representations. Second, clever uses of attention allow for the these constructions to focus on particularly relevant tokens and object (such as mentions and entities) representations. Third, aggregation of signal across mentions in entity-level RE is a key focus of research. Fourth, the injection of additional signal by adding tokens to the text prior to encoding via language model (LM) or through additional learning tasks boosts performance. Last, we explore an assortment of strategies for the challenging task of end-to-end entity-level RE. Of particular note are sequence-to-sequence (seq2seq) methods that have become particularly popular in the past few years. With the success of general-domain generative LMs, biomedical NLP researchers have trained a variety of these models on biomedical text under the assumption that they would be superior for biomedical tasks. As training such models is computationally expensive, we investigate whether they outperform generic models. We test this assumption rigorously by comparing performance of all major biomedical generative language models to the performances of their generic counterparts across multiple biomedical RE datasets, in the traditional finetuning setting as well as in the few-shot setting. Surprisingly, we found that biomedical models tended to underperform compared to their generic counterparts. However, we found that small-scale biomedical instruction finetuning improved performance to a similar degree as larger-scale generic instruction finetuning. Zero-shot natural language processing (NLP) offers savings on the expenses associated with annotating datasets and the specialized knowledge required for applying NLP methods. Large, generative LMs trained to align with human objectives have demonstrated impressive zero-shot capabilities over a broad range of tasks. However, the effectiveness of these models in biomedical RE remains uncertain. To bridge this gap in understanding, we investigate how GPT-4 performs across several RE datasets. We experiment with the recent JSON generation features to generate structured output, which we use alternately by defining an explicit schema describing the relation structure, and inferring the structure from the prompt itself. Our work is the first to study zero-shot biomedical RE across a variety of datasets. Overall, performance was lower than that of fully-finetuned methods. Recall suffered in examples with more than a few relations. Entity mention boundaries were a major source of error, which future work could fruitfully address. In our previous work with generative LMs, we noted that RE performance decreased with the number of gold relations in an example. This observation aligns with the general pattern that recurrent neural network and transformer-based model performance tends to decrease with sequence length. Generative LMs also do not identify textual mentions or group them into entities, which are valuable information extraction tasks unto themselves. Therefore, in this age of generative methods, we revisit non-seq2seq methodology for biomedical RE. We adopt a sequential framework of named entity recognition (NER), clustering mentions into entities, followed by relation classification (RC). As errors early in the pipeline necessarily cause downstream errors, and NER performance is near its ceiling, we focus on improving clustering. We match state-of-the-art (SOTA) performance in NER, and substantially improve mention clustering performance by incorporating dependency parsing and gating string dissimilarity embeddings. Overall, we advance the field of biomedical RE in a few ways. In our experiments of finetuned LMs, we show that biomedicine-specific models are unnecessary, freeing researchers to make use of SOTA generic LMs. The relatively high few-shot performance in these experiments also suggests that biomedical RE can be reasonably accessible, as it is not so difficult to construct small datasets. Our investigation into zero-shot RE shows that SOTA LMs can compete with fully finetuned smaller LMs. Together these studies also demonstrate weaknesses of generative RE. Last, we show that non-generative RE methods still outperform generative methods in the fully-finetuned setting