Evidence map›Paper›PMID 38066573›Full record

ArticleJournal of biomedical semantics2023

BioBLP: a modular framework for learning on multimodal biomedical knowledge graphs.

Daniel Daza, Dimitrios Alivanistos, Payal Mitra, Thom Pijnenburg, Michael Cochez, Paul Groth

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Article in Journal of biomedical semantics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Daniel DazaVrije Universiteit Amsterdam, Amsterdam, The Netherlands. d.dazacruz@vu.nl.
Dimitrios AlivanistosVrije Universiteit Amsterdam, Amsterdam, The Netherlands. d.alivanistos@vu.nl.
Payal MitraElsevier B.V., Amsterdam, The Netherlands.
Thom PijnenburgElsevier B.V., Amsterdam, The Netherlands.
Michael CochezVrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Paul GrothUniversity of Amsterdam, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKnowledge graphs (KGs) are an important tool for representing complex relationships between entities in the biomedical domain. Several methods have been proposed for learning embeddings that can be used to predict new links in such graphs. Some methods ignore valuable attribute data associated with entities in biomedical KGs, such as protein sequences, or molecular graphs. Other works incorporate such data, but assume that entities can be represented with the same data modality. This is not always the case for biomedical KGs, where entities exhibit heterogeneous modalities that are central to their representation in the subject domain.

objectiveWe aim to understand how to incorporate multimodal data into biomedical KG embeddings, and analyze the resulting performance in comparison with traditional methods. We propose a modular framework for learning embeddings in KGs with entity attributes, that allows encoding attribute data of different modalities while also supporting entities with missing attributes. We additionally propose an efficient pretraining strategy for reducing the required training runtime. We train models using a biomedical KG containing approximately 2 million triples, and evaluate the performance of the resulting entity embeddings on the tasks of link prediction, and drug-protein interaction prediction, comparing against methods that do not take attribute data into account.

resultsIn the standard link prediction evaluation, the proposed method results in competitive, yet lower performance than baselines that do not use attribute data. When evaluated in the task of drug-protein interaction prediction, the method compares favorably with the baselines. Further analyses show that incorporating attribute data does outperform baselines over entities below a certain node degree, comprising approximately 75% of the diseases in the graph. We also observe that optimizing attribute encoders is a challenging task that increases optimization costs. Our proposed pretraining strategy yields significantly higher performance while reducing the required training runtime.

conclusionBioBLP allows to investigate different ways of incorporating multimodal biomedical data for learning representations in KGs. With a particular implementation, we find that incorporating attribute data does not consistently outperform baselines, but improvements are obtained on a comparatively large subset of entities below a specific node-degree. Our results indicate a potential for improved performance in scientific discovery tasks where understudied areas of the KG would benefit from link prediction methods.

Indexed as

Pattern Recognition, AutomatedBiomedical knowledgeGraph embeddingsMultimodal knowledge graph

Identifiers

PMID38066573
PMCPMC10709903

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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 OpenQuestion graph.