Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_assertion description "[Among 14 870 subjects, the pooled estimated risk of stroke/TIA associated with the 677T allele increased in a dose-dependent manner (T allele pooled OR 1.17, 95%CI 1.09 to 1.26, TT genotype pooled OR 1.37, 95%CI 1.15 to 1.64).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_assertion evidence source_evidence_literature NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_assertion SIO_000772 15947278 NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_assertion wasDerivedFrom befree-20140225 NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_assertion wasGeneratedBy ECO_0000203 NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP382971.RAjH14WeXoCk1a4AMh991-pG4d1oPHTlGhndyKow9ULjQ130_provenance.