Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion type Assertion NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_head.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_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." NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_provenance.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion evidence source_evidence_literature NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_provenance.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion SIO_000772 15475941 NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_provenance.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion wasDerivedFrom befree-20140225 NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_provenance.
- NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_assertion wasGeneratedBy ECO_0000203 NP498745.RAep3kDgYqWDCqpFDOM5kOLDmPupc71nDTw2nWe9HQa0w130_provenance.