Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion> ?p ?o ?g. }
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- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion type Assertion NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_head.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_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." NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion evidence source_evidence_literature NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion SIO_000772 21088058 NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion wasDerivedFrom befree-20150227 NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.
- NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_assertion wasGeneratedBy ECO_0000203 NP257799.RA9aPQ_nkNgo19FTm8qWOCITVe2wjk0zP-FgwLjrH_o-E130_provenance.