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- source_evidence_literature type ECO_0000212 NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_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." NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_assertion evidence source_evidence_literature NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_assertion SIO_000772 22926736 NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_assertion wasDerivedFrom befree-20150227 NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_assertion wasGeneratedBy ECO_0000203 NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP282169.RAjRgMWBVXIbq3Bvy7qAwpTdAeQ0rcnNJKjJX920q4Ozw130_provenance.