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- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion type Assertion NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_head.
- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion wasGeneratedBy ECO_0000203 NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_provenance.
- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion wasDerivedFrom befree-2016 NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_provenance.
- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion SIO_000772 15264268 NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_provenance.
- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion evidence source_evidence_literature NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_provenance.
- NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_assertion description "[This article traces the historical aspects of hereditary cancer dealing with identification and ultimate molecular genetic confirmation of commonly occurring cancers, particularly of the colon in the case of familial adenomatous polyposis and its attenuated form, both due to the APC germline mutation; the Lynch syndrome due to mutations in mismatch repair genes, the most common of which were found to be MSH2, MLH1, and MSH6 germline mutations; the hereditary breast-ovarian cancer syndrome with BRCA1 and BRCA2 germline mutations; the Li-Fraumeni (SBLA) syndrome due to the p53 mutation; and the familial atypical multiple mole melanoma in association with pancreatic cancer due to the CDKN2A (p16) germline mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452713.RAD7Q_lOrDycUXRwIbOjTMZkSkh44tIRiuSUagaQznjK4130_provenance.