Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion description "[The results of this study indicate that the 9p21 variation has an impact on CDKN2A and CDKN2B expression in VSMCs and influences VMSC proliferation, which likely represents an important mechanism for the association between this genetic locus and susceptibility to CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion evidence source_evidence_literature NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion SIO_000772 22706276 NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion wasDerivedFrom befree-2016 NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion wasGeneratedBy ECO_0000203 NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.
- befree-2016 importedOn "2016-02-19" NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance.