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- source_evidence_literature type ECO_0000212 NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- befree-2016 importedOn "2016-02-19" NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_assertion wasGeneratedBy ECO_0000203 NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_assertion wasDerivedFrom befree-2016 NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_assertion SIO_000772 20697805 NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_assertion evidence source_evidence_literature NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.
- NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_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." NP831821.RA5d_CZs3E-gwbtbS1Z__E1qx37fFjqrJpBA6BXf_e3cI130_provenance.