Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion wasGeneratedBy ECO_0000203 NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion wasDerivedFrom gad-20150221 NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion SIO_000772 16298355 NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion evidence source_evidence_literature NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.
- NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_assertion description "[ While any single mutation causes only a mildly increased LR (none > 1.7), in combination, the likelihood of early-onset CAD increased to 2.78 with four mutations. The genetics of early-onset CAD appear to be multifactorial, requiring polygenic models to ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97229.RAVA-uhsN22K1SrRQl0C4rZwScC9le3Y0rfF5QA_-bX9g130_provenance.