Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_assertion description "[The index patient's phenotype was severe, manifested by classic features of the illness (adrenal insufficiency, hypoparathyroidism, candidiasis, and keratoconjunctivitis with alopecia universalis), as well as by severe exocrine pancreatic insufficiency, diabetes mellitus, hepatic inflammation, growth hormone (GH) deficiency due to lymphocytic hypophysitis, and primary ovarian failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_assertion evidence source_evidence_literature NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_assertion SIO_000772 10084559 NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_assertion wasDerivedFrom befree-2016 NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_assertion wasGeneratedBy ECO_0000203 NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.
- befree-2016 importedOn "2016-02-19" NP248004.RAgXykcM32B9NbDtsI6Wl4sAO3TsFbte7SmjMThTgFb5o130_provenance.