ArticlePharmacology research & perspectives2024
Cross-modal embedding integrator for disease-gene/protein association prediction using a multi-head attention mechanism.
Article in Pharmacology research & perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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Who cites it
2 citing papers in PubMed.
- Application and Prospects of Large Language Models in Small-Molecule Drug Discovery.Analytical chemistry · 2025Review
- Cross-modal embedding integrator for disease-gene/protein association prediction using a multi-head attention mechanism.Pharmacology research & perspectives · 2024Article
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Authors and funding
4 authors.
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Abstract
Knowledge graphs, powerful tools that explicitly transfer knowledge to machines, have significantly advanced new knowledge inferences. Discovering unknown relationships between diseases and genes/proteins in biomedical knowledge graphs can lead to the identification of disease development mechanisms and new treatment targets. Generating high-quality representations of biomedical entities is essential for successfully predicting disease-gene/protein associations. We developed a computational model that predicts disease-gene/protein associations using the Precision Medicine Knowledge Graph, a biomedical knowledge graph. Embeddings of biomedical entities were generated using two different methods-a large language model (LLM) and the knowledge graph embedding (KGE) algorithm. The LLM utilizes information obtained from massive amounts of text data, whereas the KGE algorithm relies on graph structures. We developed a disease-gene/protein association prediction model, "Cross-Modal Embedding Integrator (CMEI)," by integrating embeddings from different modalities using a multi-head attention mechanism. The area under the receiver operating characteristic curve of CMEI was 0.9662 (± 0.0002) in predicting disease-gene/protein associations. In conclusion, we developed a computational model that effectively predicts disease-gene/protein associations. CMEI may contribute to the identification of disease development mechanisms and new treatment targets.
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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 OpenQuestion graph.