Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_assertion description "[MTHFR C677T and MTRR A66G were found to increase the risk for CAD by 1.61-fold (95% CI: 1.04-2.50) and 1.92-fold (95% CI: 1.29-2.87) whereas TYMS 2R allele was found to reduce the risk for CAD (OR: 0.66, 95% CI: 0.49-0.88) by counteracting MTHFR and MTRR variant alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_assertion evidence source_evidence_literature NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_assertion SIO_000772 20962453 NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_assertion wasDerivedFrom befree-20140225 NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_assertion wasGeneratedBy ECO_0000203 NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883260.RA7R36OjmJvgQdcmmTOLxhGI-vK0GsaRr5jwlKdiLIQ60130_provenance.