Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion> ?p ?o ?g. }
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- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion type Assertion NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_head.
- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion description "[None of these tagging SNPs was associated with breast cancer risk, with the exception of XRCC2 rs3218536, R188H, which showed some evidence of a protective association for the rare allele per allele odds ratio, 0.89; 95% confidence intervals (95% CI), 0.80-0.99; P trend = 0.03.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_provenance.
- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion evidence source_evidence_literature NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_provenance.
- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion SIO_000772 19064565 NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_provenance.
- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion wasDerivedFrom gad-20150221 NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_provenance.
- NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_assertion wasGeneratedBy ECO_0000203 NP76382.RATNMSWXK3gve9e1vJeJ5Y50PPWU0uqw6ig2fDR5nEmsA130_provenance.