Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_assertion description "[We did not observe a significant association between CAD and genotypes or alleles of IL1B C(-31)T/IL1RN VNTR or their haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_assertion evidence source_evidence_literature NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_assertion SIO_000772 21840356 NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_assertion wasDerivedFrom befree-20140225 NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_assertion wasGeneratedBy ECO_0000203 NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP333189.RAz84VEIf3xpkfXR3n5R8gbWysqFVVJAHw1v7KZ80E9PI130_provenance.