Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion> ?p ?o ?g. }
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- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion type Assertion NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_head.
- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_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." NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_provenance.
- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion evidence source_evidence_literature NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_provenance.
- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion SIO_000772 7541187 NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_provenance.
- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion wasDerivedFrom befree-2016 NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_provenance.
- NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_assertion wasGeneratedBy ECO_0000203 NP1311606.RA4L1or5nFMRLhToM2zGKrCm4EkEBdmQfkKOFcQW6RM7E130_provenance.