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- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_assertion type Assertion NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_head.
- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_assertion wasGeneratedBy ECO_0000203 NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_provenance.
- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_assertion wasDerivedFrom befree-20150227 NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_provenance.
- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_assertion SIO_000772 20697805 NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_provenance.
- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_assertion evidence source_evidence_literature NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_provenance.
- NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_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." NP663903.RA2Fai-60RJIOQ9-E00ne2AOjI00UEmUndzMeOUoXATss130_provenance.