Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion> ?p ?o ?g. }
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- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion type Assertion NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_head.
- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion description "[In the multivariate logistic regression models, CTLA4 +49 A/G variant genotype was associated with increased risk (AA vs GG) by 1.43-fold (95% CI = 0.94-2.17) for HCC, and 1.66-fold (95% CI = 1.13-2.44) for cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_provenance.
- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion evidence source_evidence_literature NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_provenance.
- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion SIO_000772 20538028 NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_provenance.
- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion wasDerivedFrom befree-20140225 NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_provenance.
- NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_assertion wasGeneratedBy ECO_0000203 NP798715.RAbH6E4GCdGyvnuYhZACeIP35Mf7j7n194kEh4HR1612M130_provenance.