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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-eturtle-containers
virtrdf-hashtag
virtrdf-ifp
virtrdf-label
virtrdf-meta-entity-class
None
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About:
Congenital Nephrogenic Diabetes Insipidus
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An Entity of Type :
about:dsyn#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
dsyn
New Facet based on Instances of this Class
Attributes
Values
label
congenital nephrogenic diabetes insipidus
COEXISTS_WITH
Hypertensive disease
Kidney Failure, Chronic
Atony of bladder NOS
ASSOCIATED_WITH
Mutation
Gene Mutation
schema:identifier
c0677501
ISA
Disease
Kidney Diseases
CAUSES
Polydipsia
Polyuria
PROCESS_OF
C0030705
Family
Human
Child
Rattus norvegicus
Woman
Mus
Infant
Girls
House mice
Canis familiaris
Boys
Rats, Brattleboro
Belgians
Shiba Inu dog
is
COEXISTS_WITH
of
Advanced cancer
is
ASSOCIATED_WITH
of
Genes
water channel
AQP2
Vasopressin Receptor
Arginine Vasopressin Receptor 2
is
DIAGNOSES
of
Molecular Diagnosis
is
CAUSES
of
Mutation
AQP2
Vasopressin Receptor
Aquaporin 2
is
TREATS
of
Water
Treatment Protocols
alanosine
Argipressin|AVP
Deamino Arginine Vasopressin
Vasoconstrictor Agents
Metformin
Thiazides
Electrolyte regulation
is
AFFECTS
of
Mutation
Gene Mutation
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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