Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_assertion description "[A1166C variant of angiotensin II type 1 receptor gene is associated with severe hypertension in pregnancy independently of T235 variant of angiotensinogen gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_assertion evidence source_evidence_literature NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_assertion SIO_000772 15042429 NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_assertion wasDerivedFrom gad-20150221 NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_assertion wasGeneratedBy ECO_0000203 NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP84498.RAFMjSw9DdzN4pWJwDyfzQvQoZF3075QWmavwD52nDXLo130_provenance.