Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_assertion description "[Additionally, systematic review and meta-analysis of the literature for genetic association studies of D2 Thr92Ala polymorphism and DM2 were performed in Medline, Embase, LiLacs, and SciELO, and major meeting databases using the terms 'rs225014' odds ratio (OR) 'thr92ala' OR 'T92A' OR 'dio2 a/g'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_assertion evidence source_evidence_literature NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_assertion SIO_000772 20566590 NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_assertion wasDerivedFrom befree-20150227 NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_assertion wasGeneratedBy ECO_0000203 NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP354389.RAO4-AmR4WIxmcEm48w6f0kLjQqBPx-tt30Q7lswpH9n4130_provenance.