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- source_evidence_literature type ECO_0000212 NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_assertion description "[Deleterious and missense mutations of RAD51C have recently been suggested to modulate the individual susceptibility to hereditary breast and ovarian cancer and unselected ovarian cancer, but not unselected breast cancer (BrC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_assertion evidence source_evidence_literature NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_assertion SIO_000772 25343521 NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_assertion wasDerivedFrom befree-2016 NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_assertion wasGeneratedBy ECO_0000203 NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232387.RADrZLHRmf2FAI_VsyoYgDv0_RVOASNMYW7lfPAl4-de4130_provenance.