Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_assertion description "[We analysed the association of 14 polymorphisms located within 10 genes (TCF7L2, ENPP1, ADRB3, KCNJ11, LEPR, PPARgamma, FTO, CDKAL1, SIRT1 and HHEX) with T2D and MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_assertion evidence source_evidence_literature NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_assertion SIO_000772 20503258 NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_assertion wasDerivedFrom gad-20130706 NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_assertion wasGeneratedBy ECO_0000203 NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.
- gad-20130706 importedOn "2013-07-06" NP63951.RAHWTSM7TUOdxGt3k65dd5IdTVKKboCt5a8oeDEo0Xxbs130_provenance.