Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_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." NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_assertion evidence source_evidence_literature NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_assertion SIO_000772 22476429 NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_assertion wasDerivedFrom befree-20150227 NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_assertion wasGeneratedBy ECO_0000203 NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663821.RAIXjWo8PQ_AKyC7hUuwGETP0N-e_6kFBv2XLxPNvXVms130_provenance.