Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_assertion description "[We evaluated the effect of MDM2 SNP309 and its interaction with the p53 Arg72Pro polymorphism on pigmentary phenotypes and skin cancer risk in a nested case-control study within the Nurses' Health Study (NHS) among 219 melanoma cases, 286 squamous cell carcinoma (SCC) cases, 300 basal cell carcinoma (BCC) cases, and 873 controls, and among controls from other studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_assertion evidence source_evidence_literature NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_assertion SIO_000772 18814047 NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_assertion wasDerivedFrom befree-20140225 NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_assertion wasGeneratedBy ECO_0000203 NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173667.RAYznXwe7WvsDZ5C8Wmh3_DnGSezZTt_dB9LYlnkk-nvk130_provenance.