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- source_evidence_literature type ECO_0000212 NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_assertion description "[Consistent with published results from similar follow-up studies, we suggest that RAD51C mutations are rare events among high-risk breast cancer and breast/ovarian cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_assertion evidence source_evidence_literature NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_assertion SIO_000772 22476429 NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_assertion wasDerivedFrom befree-20150227 NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_assertion wasGeneratedBy ECO_0000203 NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663870.RAB2Yd_EC8AL2I0ivNw0eybqFPNVTKCGFXx36HbU3m34o130_provenance.