Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_assertion description "[We investigated whether putatively functional single nucleotide polymorphisms (SNPs) in genes related to CIN (CENPF, ESPL1, NEK2, PTTG1, ZWILCH, ZWINT) affect breast cancer (BC) risk and clinical outcome in a Swedish cohort of 749 incident BC cases with detailed clinical data and up to 15 years of follow-up and 1493 matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_assertion evidence source_evidence_literature NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_assertion SIO_000772 19008095 NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_assertion wasDerivedFrom befree-20150227 NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_assertion wasGeneratedBy ECO_0000203 NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP916191.RAHeXxTpA17XqcNLu10YWuzfSO5mC1HVIV2Jrlzl0GC9M130_provenance.