Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_assertion description "[C-allele carriers of the rs579459 variant, which is located upstream of the ABO gene and correlates with blood group A, were independently associated with recurrent MI [multivariable-adjusted hazard ratio (HR) 2.25, CI = 1.37-3.71; P = 0.001] and with recurrent MI or cardiac death [multivariable-adjusted (HR) 1.80, CI = 1.09-2.95; P = 0.021] within 5 years after an index ACS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_assertion evidence source_evidence_literature NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_assertion SIO_000772 23161703 NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_assertion wasDerivedFrom befree-20140225 NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_assertion wasGeneratedBy ECO_0000203 NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP200133.RAutXN2AyBNFELp7XK5Nsp7LAS6ZYWblhhQ2lkig6gemI130_provenance.