Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_assertion wasGeneratedBy ECO_0000203 NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_assertion wasDerivedFrom befree-20150227 NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_assertion SIO_000772 24822274 NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_assertion evidence source_evidence_literature NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.
- NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_assertion description "[This suggests that UGT genetic variation alters CRC risk differently by anatomical sub-site and gender and that polymorphisms in the UGT1A shared exons may have a regulatory effect on gene expression that allows for the protective effect of NSAIDs on CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765917.RASctjYa78mtN2XQrKDzda_CsTEvDI2n5KGB5e8egk5i8130_provenance.