Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_assertion description "[The -786C/T SNP of the nos-3 gene thus constitutes a genetic risk factor for CHD, presumably due to binding of an inhibitory transcription factor to the C-type promoter blocking shear stress-dependent maintenance of NOS-3 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_assertion evidence source_evidence_literature NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_assertion SIO_000772 15375006 NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_assertion wasDerivedFrom befree-20150227 NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_assertion wasGeneratedBy ECO_0000203 NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP692525.RAwDD_3yv3qi4GBArQgVwrmx46tNy-nhulIea3yqbCuQk130_provenance.