Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion> ?p ?o ?g. }
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- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion type Assertion NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_head.
- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion description "[To verify the S305N association with melanoma risk in an independent larger French population (378 patients, 389 controls); to investigate the role of EDNRB variants in melanoma risk in an Italian population (133 patients, 118 controls); and to explore the association of CDKN2A or CDK4 mutations with the S305N EDNRB variant in a subgroup of patients (59 French, 12 Italian) with a suspected hereditary predisposition to melanoma (familial melanoma, sporadic multiple primary melanoma or melanoma associated with pancreatic cancer).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_provenance.
- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion evidence source_evidence_literature NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_provenance.
- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion SIO_000772 21507037 NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_provenance.
- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion wasDerivedFrom befree-20150227 NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_provenance.
- NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_assertion wasGeneratedBy ECO_0000203 NP301468.RAWtAnIwzqC_Qo6rUKKngWnEueAQnl0cha_jtFmWPTTWA130_provenance.