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- NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_assertion type Assertion NP1018286.RADeWIsak1HGHGTrB1fTJWqit73TovQ1pmwBLKOXD2Q1s130_head.
- 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.