Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_assertion wasGeneratedBy ECO_0000203 NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_assertion wasDerivedFrom gad-20150221 NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_assertion SIO_000772 18679013 NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_assertion evidence source_evidence_literature NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.
- NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_assertion description "[MtSNPs T3394C in NADH dehydrogenase subunit 1 (ND1), G4491A in ND2, T16189C and T16519C were found with significantly higher frequency in patients with T2DM than in the controls (T16189C, p = 0.0045; T16519C, p < 0.0001; T3394C, p = 0.0015; G4491A, p = 0.0015).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95442.RApI76HTWk2Tph6tBXdxggsNC0NXUnNT4mu-4YLr0gEfw130_provenance.