Evidence map›Paper›PMID 42640507›Full record

ArticleBioinformatics (Oxford, England)2026

RGCNMDA: pathway-bridged relational graph learning with adaptive multi-view fusion for human miRNA-disease association prediction.

Chao Hou, Mohamed Kone, Yang Xiang, Shulin Wang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Chao HouCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, Hunan 410082, China.ORCID 0009-0006-4650-8258
Mohamed KoneCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, Hunan 410082, China.
Yang XiangCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, Hunan 410082, China.
Shulin WangCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, Hunan 410082, China.

Funding

National Natural Science Foundation of China: Stochastic dynamics model of somatic mutations affecting cancer 61672011
6 · The paper itself

Abstract

motivationMicroRNAs are key post-transcriptional regulators whose dysregulation is associated with complex human diseases. Computational prediction can prioritize candidate miRNA-disease associations, but reliable evaluation is complicated by sparse labels, cold-start entities, limited biological context in bipartite graphs, and leakage when association-derived features are constructed before data splitting.

resultsWe present RGCNMDA, a leakage-controlled multi-view framework that integrates global latent structure, local profiles and similarities, and pathway context. Within every fold, interaction profiles, GIP similarities, PCA inputs, MDMF factors, and miRNA-disease graph edges are reconstructed exclusively from training positives. Four independent factorized encoders transform the miRNA and disease interaction profiles and GIP similarities, while a fold-local MDMF branch captures global latent structure. These representations are integrated with a pathway-bridged graph containing miRNA, disease, and pathway nodes connected by six directed relation types. A relational graph convolutional network performs type- and direction-specific message passing, and node-wise gates adaptively fuse graph, MDMF, and combined profile and similarity representations before an MLP pair decoder scores candidate associations. On HMDD v4.0, RGCNMDA achieved AUCs of 0.9589, 0.9109, and 0.8836 under random, cold-disease, and cold-miRNA evaluation, respectively; on the processed independent-source RNADisease v4.0 benchmark, the corresponding values were 0.9580, 0.8446, and 0.8913. Same-protocol baseline comparisons and diagnostic analyses showed that the benefits of RGCNMDA were setting dependent, with the strongest pathway-related improvement under cold-disease evaluation. These results support the robustness of leakage-controlled multi-view learning across standard and cold-start evaluation settings. AVAILABILITY AND IMPLEMENTATION: https://github.com/hnuchao/pathway-RGCNMDA.

Indexed as

Computational BiologyDiseaseMicroRNAsSoftwareAlgorithmsGraph Neural NetworksHumansMicroRNAs

Identifiers

PMID42640507
PMCPMC13544353

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.