Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_assertion description "[Genotyping of HPC2/ELAC2 variants (S217L, A541T), along with RNASEL variants (R462Q and E541D) was completed in 155 African American sporadic and 88 familial prostate cancer cases, and 296 healthy male controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_assertion evidence source_evidence_literature NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_assertion SIO_000772 18767027 NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_assertion wasDerivedFrom befree-2016 NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_assertion wasGeneratedBy ECO_0000203 NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.
- befree-2016 importedOn "2016-02-19" NP691187.RATmRDq8s37e5LkeE30F82FMWqMbPNyxsiALeoBsBdUpI130_provenance.