Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion> ?p ?o ?g. }
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- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion type Assertion NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_head.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_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." NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion evidence source_evidence_literature NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion SIO_000772 21088058 NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion wasDerivedFrom befree-20140225 NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.
- NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_assertion wasGeneratedBy ECO_0000203 NP192363.RAJhDq9k1wrewPHglfRvqvCei615IAnu4hEN3Vf0cw0cA130_provenance.