Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_assertion wasGeneratedBy ECO_0000203 NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_assertion wasDerivedFrom befree-20140225 NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_assertion SIO_000772 21734245 NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_assertion evidence source_evidence_literature NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_assertion description "[Hypomorphic mutations in the X-linked NEMO gene and hypermorphic mutations in the autosomal IKBA gene cause X-linked recessive and autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435678.RANyI3YVvWf6aa3zDu2Tjt03TnHM_iqUlLMhQ7cKQOrBU130_provenance.