Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion description "[Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI), a disorder caused by mutations in the vasopressin (AVP)-neurophysin II (NPII) gene, manifests gradually during early childhood with progressive polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion evidence source_evidence_literature NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion SIO_000772 21088058 NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion wasDerivedFrom befree-20140225 NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_assertion wasGeneratedBy ECO_0000203 NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615822.RAqejoMEjYl-e9LEqJfP7jqRPn3Ym1ihukVZFUnExxP2E130_provenance.