Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_assertion description "[Genetic variation in GCH1 underlies important differences in endogenous BH4 availability and is a determinant of eNOS coupling, vascular redox state, and endothelial function in human vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_assertion evidence source_evidence_literature NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_assertion SIO_000772 18598896 NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_assertion wasDerivedFrom befree-20150227 NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_assertion wasGeneratedBy ECO_0000203 NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420560.RA5i8sr7Re6xEfCu8B1JXN1e2Aubr9lXuX1VGEe9-NloA130_provenance.