Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion> ?p ?o ?g. }
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- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion type Assertion NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_head.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion description "[Three different inheritance patterns have been described, i.e., the X-linked recessive form associated with arginine vasopressin V2 receptor (AVPR2) gene mutations, the autosomal recessive and dominant forms of CNDI associated with mutations in the aquaporin-2 (AQP2) gene encoding the vasopressin-regulated water channel of the renal collecting duct.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion evidence source_evidence_literature NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion SIO_000772 19461158 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion wasDerivedFrom befree-20150227 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.
- NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_assertion wasGeneratedBy ECO_0000203 NP257891.RAgN2r2meRcvYhy2Q7kKh_SP-ojCF_ABpOXekRInIwkWk130_provenance.