Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion> ?p ?o ?g. }
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- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion type Assertion NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_head.
- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion description "[We have demonstrated the utility of this strategy in two different hereditary colorectal cancer syndromes, one caused by a defective tumour suppressor gene on chromosome 5 (familial adenomatous polyposis, FAP) and the other caused by a defective mismatch repair gene on chromosome 2 (hereditary non-polyposis colorectal cancer, HNPCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_provenance.
- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion evidence source_evidence_literature NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_provenance.
- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion SIO_000772 7550326 NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_provenance.
- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion wasDerivedFrom befree-2016 NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_provenance.
- NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_assertion wasGeneratedBy ECO_0000203 NP1312174.RAeMTZz9PpezP5eOkitfSvQv1hFoCxSjh6wDcMhr-NmWw130_provenance.