Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_assertion description "[Although association was detected between SCGB3A2 and U.K. Caucasian GD subjects, the size of effect was smaller than that seen in the Oriental population (odds ratio = 1.28-1.73).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_assertion evidence source_evidence_literature NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_assertion SIO_000772 20210668 NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_assertion wasDerivedFrom gad-20150221 NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_assertion wasGeneratedBy ECO_0000203 NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP166891.RAzotGLXJFYqJOxBNSsvj6H4HgiSBt85CPRpS_HzQbSmo130_provenance.