Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion> ?p ?o ?g. }
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- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion type Assertion NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_head.
- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion description "[Carriers of the variant XPD 751Gln allele had an increased risk of low-risk adenomas (OR 1.40, 95% CI 1.03-1.89), while no association was found with risk of carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_provenance.
- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion evidence source_evidence_literature NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_provenance.
- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion SIO_000772 16542436 NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_provenance.
- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion wasDerivedFrom befree-20140225 NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_provenance.
- NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_assertion wasGeneratedBy ECO_0000203 NP441784.RAwMsk2Fj_JwMVfJ0N8EJ0ZQS9De9NoShZPdkx97axBE4130_provenance.