Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1302753.RA-S34LXqmzMQpYqN8wT3zUVwShVZZuEyy_ezK9rzGoNQ#provenance>. }
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- source_evidence_literature type ECO_0000212 provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." provenance.
- GAD importedOn "2017-02-21" provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom GAD provenance.
- assertion SIO_000772 20942809 provenance.
- assertion evidence source_evidence_literature provenance.
- 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." provenance.