Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_assertion description "[The aim of the present study was to find a relationship between 561A > C and 98G > T polymorphisms of E-selectin gene and CAD as well as interactions between these polymorphic variants and traditional risk factors of the disease in determining the susceptibility to CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_assertion evidence source_evidence_literature NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_assertion SIO_000772 18649056 NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_assertion wasDerivedFrom befree-20140225 NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_assertion wasGeneratedBy ECO_0000203 NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471793.RAUkAPvD1rF8PwEaY3mubk1dLP8RcEAcJ-F5qFwrGSkDs130_provenance.