Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_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." NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_assertion evidence source_evidence_literature NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_assertion SIO_000772 22706276 NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_assertion wasDerivedFrom befree-2016 NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_assertion wasGeneratedBy ECO_0000203 NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.
- befree-2016 importedOn "2016-02-19" NP990808.RAQ_34uujFtQL5RF8E85UeU8ktUfhSzkRdJC_CaE6KPKA130_provenance.