Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_assertion description "[The Intermountain Healthcares Coronary Genetics study demonstrates the ability of a multigenic, multipathway GRS to improve discrimination of angiographic CAD. Genetic risk scores promise to increase understanding of the genetic basis of CAD and improve identification of individuals at increased CAD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_assertion evidence source_evidence_literature NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_assertion SIO_000772 20691829 NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_assertion wasDerivedFrom gad-20130706 NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_assertion wasGeneratedBy ECO_0000203 NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP75714.RAGDv5bQfI3-eh8IrX5-pAgbvT-RRZI0vgg1Hf7OidORk130_provenance.