Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion wasGeneratedBy ECO_0000203 NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion wasDerivedFrom befree-20150227 NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion SIO_000772 17319270 NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion evidence source_evidence_literature NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.
- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion description "[CBS gene G919A mutation is associated with the development of CHD, and the mutated allele may decrease the risk of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_provenance.