Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_assertion description "[The aim of the study is to investigate the relevance of rs1056663 and rs2708861 HUS1 polymorphisms, and rs104548, rs2981582 and rs2910164 polymorphisms of CASP8, FGFR2 and micro RNA 146A genes, respectively, as risk modifiers in hereditary breast or ovarian cancer (BC/OC) and risk factors in sporadic BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_assertion evidence source_evidence_literature NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_assertion SIO_000772 22926736 NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_assertion wasDerivedFrom befree-20140225 NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_assertion wasGeneratedBy ECO_0000203 NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755836.RA_-0ekWLB1uoO00lIscIzPH4KQKszHuBgeSakmSYuM1A130_provenance.