Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion type Assertion NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_head.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion description "[The identification, characterization, and mutational analysis of three different genes, namely the prepro-arginine-vasopressin-neurophysin II gene (prepro-AVP-NPII), the arginine-vasopressin receptor 2 gene (AVPR2), and the vasopressin-sensitive water channel gene (aquaporin-2, AQP2), provide the basis for our understanding of three different hereditary forms of diabetes insipidus: autosomal dominant neurogenic diabetes insipidus, X-linked nephrogenic diabetes insipidus, and autosomal recessive nephrogenic diabetes insipidus, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_provenance.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion evidence source_evidence_literature NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_provenance.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion SIO_000772 7541187 NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_provenance.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion wasDerivedFrom befree-2016 NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_provenance.
- NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_assertion wasGeneratedBy ECO_0000203 NP1311611.RAV02oEFeb9tpdym3nq8FgnUqgSPKqZtgOxp91H17zLCc130_provenance.