ArticleBriefings in bioinformatics2024
BioGSF: a graph-driven semantic feature integration framework for biomedical relation extraction.
Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
3 citing papers in PubMed.
- Integrated computational and experimental approaches for drug repurposing targeting key Mycobacterium tuberculosis proteins.Molecular diversity · 2026Article
- A parallel dual-stream state-space module for reliable and efficient biomedical relation extraction.PLoS computational biology · 2026Article
- ACP-EPC: an interpretable deep learning framework for anticancer peptide prediction utilizing pre-trained protein language model and multi-view feature extracting strategy.Molecular diversity · 2026Article
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Authors and funding
5 authors.
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Abstract
The automatic and accurate extraction of diverse biomedical relations from literature constitutes the core elements of medical knowledge graphs, which are indispensable for healthcare artificial intelligence. Currently, fine-tuning through stacking various neural networks on pre-trained language models (PLMs) represents a common framework for end-to-end resolution of the biomedical relation extraction (RE) problem. Nevertheless, sequence-based PLMs, to a certain extent, fail to fully exploit the connections between semantics and the topological features formed by these connections. In this study, we presented a graph-driven framework named BioGSF for RE from the literature by integrating shortest dependency paths (SDP) with entity-pair graph through the employment of the graph neural network model. Initially, we leveraged dependency relationships to obtain the SDP between entities and incorporated this information into the entity-pair graph. Subsequently, the graph attention network was utilized to acquire the topological information of the entity-pair graph. Ultimately, the obtained topological information was combined with the semantic features of the contextual information for relation classification. Our method was evaluated on two distinct datasets, namely S4 and BioRED. The outcomes reveal that BioGSF not only attains the superior performance among previous models with a micro-F1 score of 96.68% (S4) and 96.03% (BioRED), but also demands the shortest running times. BioGSF emerges as an efficient framework for biomedical RE.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.