Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_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 i]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_assertion evidence source_evidence_literature NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_assertion SIO_000772 20691829 NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_assertion wasDerivedFrom gad-20150221 NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_assertion wasGeneratedBy ECO_0000203 NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.
- gad-20150221 importedOn "2015-02-21" NP183354.RAGrwWGxL4cDxqdXKsJcf1ptct7AW0DW2Ke5EYmeDR2-E130_provenance.