Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_assertion wasGeneratedBy ECO_0000203 NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_assertion wasDerivedFrom lhgdn-20090331 NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_assertion SIO_000772 17512363 NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_assertion evidence source_evidence_literature NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.
- NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_assertion description "[multiple, less common SNPs and haplotype variants underlie CETP-related coronary artery disease risk; occurrence of risk-related variants on separate haplotypes suggests genetic-risk complexity and allelic heterogeneity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225386.RA5mcsfStnw_xeJZMfvsxfpssFyHxpqsDJi6-SN7znV5M130_provenance.