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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
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None
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"Same As":
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About:
Alport Syndrome, X-Linked
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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
alport syndrome, x-linked
COEXISTS_WITH
Disease
Carrier of disorder
ASSOCIATED_WITH
Mutation
schema:identifier
c1567742
ISA
Disease
Kidney Diseases
Hereditary Diseases
Collagen Diseases
Hereditary nephritis
PROCESS_OF
C0030705
Family
Females
Males
Woman
Male population group
Mus
Canis familiaris
Brothers
Boys
sibling
Mice, Transgenic
Adolescent
Sister
Twin brother
AFFECTS
Endocytosis
is
LOCATION_OF
of
Labyrinth
Epidermal basement zone
is
COEXISTS_WITH
of
Nephritis
Leiomyomatosis
is
ASSOCIATED_WITH
of
hearing impairment
Collagen Gene
Collagen Type IV
Genotype
COL4A5|SLC2A10
COL4A5 gene|COL4A5
is
DIAGNOSES
of
Polymerase Chain Reaction
Immunohistochemistry
Functional assessment
is
CAUSES
of
Mutation
Gene Mutation
Mutation, Missense
Embryonic Mosaic
Mutation, Nonsense
COL4A5|SLC2A10
is
TREATS
of
Therapeutic procedure
Detection
follow-up
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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