Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_assertion description "[The multivariate model included 512 men with coronary artery disease from the REGRESS study who were completely genotyped for eight polymorphisms selected in the univariate procedure (ie, APOA1 G(-75)A, ABCA1 C(-477)T, ABCA1 G1051A, APOC3 T3206G, APOE Arg158Cys, LIPC C(-514)T, LPL Asn291Ser and LPL Ser447Stop).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_assertion evidence source_evidence_literature NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_assertion SIO_000772 15657615 NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_assertion wasDerivedFrom befree-2016 NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_assertion wasGeneratedBy ECO_0000203 NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.
- befree-2016 importedOn "2016-02-19" NP476822.RAE0PW11wwqm40CoRuceFCx0z54iw5p0MkXEizvrb_tco130_provenance.