Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion> ?p ?o ?g. }
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- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion type Assertion NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_head.
- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion description "[Our best-fitting model showed significant and independent effects of the PI1-deficient allele (odds ratio [OR], 2.0; 95% confidence interval [CI], 1.4 to 3.0) and the ELA2 T-G haplotype (OR, 4.1; 95% CI, 1.9 to 8.9) on lung cancer risk, and an increased risk (OR, 2.6; 95% CI, 2.4 to 2.8) for individuals carrying both a PI1-deficient allele and a G-G haplotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_provenance.
- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion evidence source_evidence_literature NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_provenance.
- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion SIO_000772 16002971 NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_provenance.
- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion wasDerivedFrom befree-20140225 NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_provenance.
- NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_assertion wasGeneratedBy ECO_0000203 NP880693.RAhXnK_cG5akb2isx53X1HYMnEytn_MF5-qLK3erUubVA130_provenance.