Evidence map›Paper›PMID 39832275›Full record

ArticleBioinformatics (Oxford, England)2025

A comprehensive graph neural network method for predicting triplet motifs in disease-drug-gene interactions.

Chuanze Kang, Zonghuan Liu, Han Zhang

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Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Chuanze KangCollege of Artificial Intelligence, Nankai University, Tianjin 300350, China.ORCID 0000-0003-4635-523X
Zonghuan LiuCollege of Artificial Intelligence, Nankai University, Tianjin 300350, China.
Han ZhangCollege of Artificial Intelligence, Nankai University, Tianjin 300350, China.ORCID 0000-0001-8498-3451

Funding

National Natural Science Foundation of China 92470124
6 · The paper itself

Abstract

motivationThe drug-disease, gene-disease, and drug-gene relationships, as high-frequency edge types, describe complex biological processes within the biomedical knowledge graph. The structural patterns formed by these three edges are the graph motifs of (disease, drug, gene) triplets. Among them, the triangle is a steady and important motif structure in the network, and other various motifs different from the triangle also indicate rich semantic relationships. However, existing methods only focus on the triangle representation learning for classification, and fail to further discriminate various motifs of triplets. A comprehensive method is needed to predict the various motifs within triplets, which will uncover new pharmacological mechanisms and improve our understanding of disease-gene-drug interactions. Identifying complex motif structures within triplets can also help us to study the structural properties of triangles.

resultsWe consider the seven typical motifs within the triplets and propose a novel graph contrastive learning-based method for triplet motif prediction (TriMoGCL). TriMoGCL utilizes a graph convolutional encoder to extract node features from the global network topology. Next, node pooling and edge pooling extract context information as the triplet features from global and local views. To avoid the redundant context information and motif imbalance problem caused by dense edges, we use node and class-prototype contrastive learning to denoise triplet features and enhance discrimination between motifs. The experiments on two different-scale knowledge graphs demonstrate the effectiveness and reliability of TriMoGCL in identifying various motif types. In addition, our model reveals new pharmacological mechanisms, providing a comprehensive analysis of triplet motifs. AVAILABILITY AND IMPLEMENTATION: Codes and datasets are available at https://github.com/zhanglabNKU/TriMoGCL and https://doi.org/10.5281/zenodo.14633572.

Indexed as

Computational BiologyDiseaseNeural Networks, ComputerAlgorithmsGraph Neural NetworksHumans

Identifiers

PMID39832275
PMCPMC11796092

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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.