Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion> ?p ?o ?g. }
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- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion type Assertion NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_head.
- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion wasGeneratedBy ECO_0000203 NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_provenance.
- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion wasDerivedFrom befree-20140225 NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_provenance.
- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion SIO_000772 20697805 NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_provenance.
- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion evidence source_evidence_literature NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_provenance.
- NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_assertion description "[It has been reported that one biallelic missense mutation in the RAD51C gene was found in a Fanconi anemia-like disorder and six monoallelic pathogenic mutations were identified in 480 BRCA1/2 negative breast and ovarian cancer pedigrees but not in 620 pedigrees with breast cancer only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644419.RAeujVBVL8QDpZ2bcExYIBMVNLuX-FLEDBP1WCkCH2oVY130_provenance.