Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_assertion description "[The C allele at SNP rs806365 (frequency, 57.4%), ~4.1 kb 3' from CNR1, was associated with increased HOMA(IR) (n = 2,261, ? = 0.05 per C, empirical P = 0.01), risk of T2D (674 cases, odds ratio = 1.19 per C, nominal P = 0.01) and CHD (237 cases, hazard ratio = 1.23 per C, nominal P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_assertion evidence source_evidence_literature NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_assertion SIO_000772 21633404 NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_assertion wasDerivedFrom befree-20140225 NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_assertion wasGeneratedBy ECO_0000203 NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900658.RAzpOynhMDSiY-c8i5rnCam9cLvYvv6-pnH-m6gtWe7vI130_provenance.