Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion> ?p ?o ?g. }
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- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion type Assertion NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_head.
- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion description "[Adjustment for prevalent and incident diabetes attenuated the association of the TSPAN8 variant (1.06, 0.99-1.13) and the genetic score (1.05, 0.99-1.12 per score tertile) with CHD risk, but not that of the CDKN2A/B variant (1.11, 1.05-1.18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_provenance.
- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion evidence source_evidence_literature NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_provenance.
- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion SIO_000772 21638130 NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_provenance.
- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion wasDerivedFrom befree-20140225 NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_provenance.
- NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_assertion wasGeneratedBy ECO_0000203 NP685705.RA-_NmD37SaPAwh-d8IIHRoa97fqdfZ8GLf-GjVmEi5M4130_provenance.