Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion> ?p ?o ?g. }
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- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion type Assertion NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_head.
- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_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." NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_provenance.
- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion evidence source_evidence_literature NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_provenance.
- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion SIO_000772 21633404 NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_provenance.
- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion wasDerivedFrom befree-20140225 NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_provenance.
- NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_assertion wasGeneratedBy ECO_0000203 NP588064.RAFQ170ew2JpKVZGMIjq3XiEaKKI9Mh0SlVi_jHMeJQgQ130_provenance.