Abstract
AbstractMotivationWhile link prediction methods in knowledge graphs have been increasingly utilized to locate potential associations between compounds and diseases, they suffer from lack of sufficient evidence to explain why a drug and a disease may be indicated. This is especially true for knowledge graph embedding (KGE) based methods where a drug-disease indication is linked only by information gleaned from a vector representation. Complementary pathwalking algorithms can increase the confidence of drug repositioning candidates by traversing a knowledge graph. However, these methods heavily weigh the relatedness of drugs, through their targets, pharmacology or shared diseases. Furthermore, these methods rely on arbitrarily extracted paths as evidence of a compound to disease indication and lack the ability to make predictions on rare diseases.ResultsIn this paper, we evaluate seven link prediction methods on a vast biomedical knowledge graph for drug repositioning. We follow the principle of consilience, and combine the reasoning paths and predictions provided by path-based and KGE methods to not only demonstrate a significant ranking performance improvement but also identify putative drug repositioning indications. Finally, we highlight the utility of our approach through a potential repositioning indication.AvailabilityThe MIND dataset can be found at 10.5281/zenodo.8117748. The python code to reproduce the entirety of this analysis can be found athttps://github.com/SuLab/{KnowledgeGraphEmbedding, CBRonMRN}.ContactAndrew I. Su atasu@scripps.eduSupplementary informationSupplementary data are available atThe Journal Titleonline.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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