Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_assertion description "[These include the contribution of variants of the regulator of G protein signaling (RGS) protein to hypertension; the role variants of the activator of G protein signaling (AGS) proteins to phenotypes (such as the type III AGS8 variant to hypoxia); the contribution of G protein-coupled receptor kinase (GRK) proteins, such as GRK4, in disorders such as hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_assertion evidence source_evidence_literature NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_assertion SIO_000772 25150869 NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_assertion wasDerivedFrom befree-2016 NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_assertion wasGeneratedBy ECO_0000203 NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1213125.RAe6w3hMApJasf1iHKqMl9nEQTmFNpid-tQIQ2zJhyIeo130_provenance.