Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion> ?p ?o ?g. }
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- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion type Assertion NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_head.
- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_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." NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_provenance.
- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion evidence source_evidence_literature NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_provenance.
- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion SIO_000772 21638130 NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_provenance.
- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion wasDerivedFrom befree-20140225 NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_provenance.
- NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_assertion wasGeneratedBy ECO_0000203 NP453865.RAcrPRfRmIPZkKw4CC0eLthKeBP2v_zeg_fRS23MwIebg130_provenance.