Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion> ?p ?o ?g. }
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- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion type Assertion NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_head.
- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion wasGeneratedBy ECO_0000203 NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_provenance.
- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion wasDerivedFrom befree-20150227 NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_provenance.
- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion SIO_000772 17935271 NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_provenance.
- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion evidence source_evidence_literature NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_provenance.
- NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_assertion description "[This review reports the most characteristic hereditary cancer syndromes along with their phenotypical and genetic variables that have been described, but it mainly focuses on Hereditary Non-Polyposis Colorectal Cancer (HNPCC), which is linked to pathogenic mutations in one of the mismatch repair (MMR) genes MLH1, MSH2, MSH6, Familial Adenomatous Polyposis (FAP) caused by high-penetrant mutations within the APC gene and Hereditary Breast/Ovarian Cancer (HBOC) linked to mutations within BRCA1 and BRCA2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569904.RAAPNdSxu7NMcqTcMfj2xEI7gARrApLBzqC8OO08DYsI8130_provenance.