Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion> ?p ?o ?g. }
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- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion type Assertion NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_head.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_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." NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion evidence source_evidence_literature NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion SIO_000772 21088058 NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion wasDerivedFrom befree-20140225 NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.
- NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_assertion wasGeneratedBy ECO_0000203 NP651673.RA88x0c8sHwZ6q0kpviO7JL0MsuMYN-91_ILreqGtP4u4130_provenance.