Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_assertion description "[In a hospital-based, case-control study of 602 non-Hispanic white CMM patients and 603 cancer-free age- and sex-matched control subjects, we genotyped FAS-1377G>A, FAS-670A>G, FASLG-844T>C and FASLG-IVS2nt-124G>A polymorphisms and assessed their respective associations with CMM risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_assertion evidence source_evidence_literature NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_assertion SIO_000772 16538172 NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_assertion wasDerivedFrom befree-20140225 NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_assertion wasGeneratedBy ECO_0000203 NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.
- befree-20140225 importedOn "2014-02-25" NP507007.RAQv_9YPuLkbL0qC0WCFnDbpBlTB-1oiiGr0OsvaTOV30130_provenance.