Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_assertion description "[The frequency of the 106 base pair allele was significantly increased in the groups of English patients with either non-associated Addison's disease or APS2 (P = 0.02 and 0.04, respectively), when compared to healthy controls with no clinical evidence or family history of either Addison's disease or any other autoimmune disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_assertion evidence source_evidence_literature NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_assertion SIO_000772 10197076 NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_assertion wasDerivedFrom befree-20140225 NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_assertion wasGeneratedBy ECO_0000203 NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP501695.RAidmgJo2onyfTTD38GEJqMf-_mwM4h0f9buDNQy_jGIQ130_provenance.