Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- befree-20150227 importedOn "2015-02-27" NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_assertion wasGeneratedBy ECO_0000203 NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_assertion wasDerivedFrom befree-20150227 NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_assertion SIO_000772 20942809 NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_assertion evidence source_evidence_literature NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.
- NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_assertion description "[The -3279CA genotype was more frequent in patients with GD in remission than in patients with intractable GD, and the -3279AA genotype, which correlates to defective transcription of FOXP3, was absent in patients with GD in remission.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899403.RAjPCCujwz2iimjwnon-l6xkhsoo82M8m9L-Nmc3cgX60130_provenance.