Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion wasGeneratedBy ECO_0000203 NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion wasDerivedFrom gad-20130706 NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion SIO_000772 17624602 NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion evidence source_evidence_literature NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_assertion description "[Our findings show that few patients with BC and CMM who lacked family histories of these cancers are carriers of deleterious germline mutations in four of the five genes we examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP59774.RApNOoLnfILdlpDxHHoSMjChuSrMCMe_2wKHMzptaOwYM130_provenance.