Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_assertion description "[A cohort of 1,575 BRCA1 and 856 BRCA2 mutation carriers was used to evaluate haplotypes at ATM, BARD1, BRIP1, CTIP, MRE11, NBS1, RAD50, RAD51, and TOPBP1 in ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_assertion evidence source_evidence_literature NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_assertion SIO_000772 19584272 NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_assertion wasDerivedFrom gad-20150221 NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_assertion wasGeneratedBy ECO_0000203 NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.
- gad-20150221 importedOn "2015-02-21" NP126395.RATr3vnWy69W90h9NI4vdfCThapIauednMpeHFW91sQos130_provenance.