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- source_evidence_literature type ECO_0000212 NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_assertion description "[These results suggest that TCF7L2 variants rs7903146 rs12255372, and rs11196205 are significantly associated with angiographically diagnosed CAD, specifically in patients with T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_assertion evidence source_evidence_literature NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_assertion SIO_000772 21423583 NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_assertion wasDerivedFrom befree-2016 NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_assertion wasGeneratedBy ECO_0000203 NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.
- befree-2016 importedOn "2016-02-19" NP881197.RAjtY-grQSogGww-epYaxNmSGQ_k71kHGoOz0mIm-yztA130_provenance.