Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_assertion description "[Although there was a tendency toward an increased number of the genotype TT of the 5-HT6 receptor polymorphism in AD patients when compared to controls (2.8% vs. 1.3%), neither this nor the 5-HT2A promoter polymorphism showed significant differences in their genotypic or allelic distribution among patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_assertion evidence source_evidence_literature NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_assertion SIO_000772 11725820 NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_assertion wasDerivedFrom gad-20150221 NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_assertion wasGeneratedBy ECO_0000203 NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP72083.RA_Zdmylz5aXMvM2kPnblcm7UKioK7S-K1IbAnP82rnCM130_provenance.