Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_assertion description "[While the common APOE polymorphism explains the majority of the locus genetic determinants of plasma lipid levels, additional SNPs in the APOC1/C2 region may contribute to CHD risk, but these effects require confirmation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_assertion evidence source_evidence_literature NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_assertion SIO_000772 20498921 NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_assertion wasDerivedFrom gad-20150221 NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_assertion wasGeneratedBy ECO_0000203 NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP177015.RA50O0dVzIF6B2p3h0nsIOchjUjGPlf6fmwVZFOMIwrJ4130_provenance.