Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion> ?p ?o ?g. }
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- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion type Assertion NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_head.
- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_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." NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_provenance.
- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion evidence source_evidence_literature NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_provenance.
- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion SIO_000772 15475941 NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_provenance.
- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion wasDerivedFrom befree-2016 NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_provenance.
- NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_assertion wasGeneratedBy ECO_0000203 NP463980.RAPHSsXQToRuqsL_FSVsk5AxJxoFu6NPwt4qcuQQAYDkM130_provenance.