Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_assertion description "[Of 19 subjects with a RAF1 mutation in two hotspots, 18 (or 95%) showed hypertrophic cardiomyopathy (HCM), compared with the 18% prevalence of HCM among individuals with Noonan syndrome in general.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_assertion evidence source_evidence_literature NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_assertion SIO_000772 17603483 NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_assertion wasDerivedFrom befree-20140225 NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_assertion wasGeneratedBy ECO_0000203 NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP708122.RAHTyWx0bIHUUJT6AdDbc6lVzHf9XQ8zCdET9cOIKprQk130_provenance.