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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
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virtrdf-ifp
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None
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About:
Walker-Warburg congenital muscular dystrophy
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An Entity of Type :
about:cgab#this
, within Data Space :
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associated with source
document(s)
Type:
cgab
New Facet based on Instances of this Class
Attributes
Values
label
walker-warburg congenital muscular dystrophy
COEXISTS_WITH
Autosome Disorders
schema:identifier
c0265221
ISA
Disease
Muscular Dystrophies
Congenital muscular dystrophy
Congenital Disorders
Lissencephaly
PART_OF
C0030705
Human
Child
Individual
Infant
Infant, Newborn
sibling
AFFECTS
Mutation
neuronal migration
MANIFESTATION_OF
Mutation
is
LOCATION_OF
of
Brain
Eye
Human
Ethnic group
is
COEXISTS_WITH
of
Congenital Abnormality
Degenerative abnormality
Fukuyama congenital muscular dystrophy
Muscular Dystrophies
Congenital muscular dystrophy
Sensorineural Hearing Loss
Pathological Dilatation
Hydrophthalmos
Testicular dysplasia
is
ASSOCIATED_WITH
of
LIS1 protein
is
DIAGNOSES
of
Prenatal Diagnosis
is
CAUSES
of
RAB18
RAB3GAP1
POMGNT2
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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