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- source_evidence_literature type ECO_0000212 NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_assertion description "[To determine the incidence of copy number variants in cancer predisposition genes from families in the Wessex region, we have analysed the hMLH1 and hMSH2 genes in patients with hereditary nonpolyposis colorectal cancer (HNPCC), BRCA1 and BRCA2 in families with hereditary breast/ovarian cancer (BRCA) and APC in patients with familial adenomatous polyposis coli (FAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_assertion evidence source_evidence_literature NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_assertion SIO_000772 15475941 NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_assertion wasDerivedFrom befree-20140225 NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_assertion wasGeneratedBy ECO_0000203 NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP403474.RAnp5QWWuyHjzVB0UnhUJx3CuE-QlRcb3kmfiaFtlQazU130_provenance.