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Rule:
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:
Atrophia bulborum hereditaria
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An Entity of Type :
about:cgab#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
dsyn
cgab
New Facet based on Instances of this Class
Attributes
Values
label
atrophia bulborum hereditaria
COEXISTS_WITH
Retinal Detachment
ASSOCIATED_WITH
Translation, Genetic
schema:identifier
c0266526
ISA
Disease
Symptoms
Congenital Abnormality
Vascular Diseases
PART_OF
osteosarcoma
CAUSES
Disease
Symptoms
Retinal Detachment
Atrophic
Deafness
PROCESS_OF
C0030705
Family
Males
Individual
Mus
Infant
Infant, Premature
Older sibling
is
LOCATION_OF
of
Extracellular Matrix
Eye
Retina
Blood supply aspects
Entire vitreous body
11q13
is
COEXISTS_WITH
of
Mental Retardation
Retinal Detachment
Congenital Abnormality
Epilepsy
Impaired cognition
Sensorineural Hearing Loss
Blind Vision
Neurologic Manifestations
Deafness
Retinal Neovascularization
Congenital blindness
Heredity
Familial exudative vitreoretinopathy
Retinoschisis
is
NEG_AFFECTS
of
Monoamine Oxidase
is
ASSOCIATED_WITH
of
Genes
Wound Healing
hearing impairment
Glutamine
Phenotype
Codon, Initiator
Candidate Disease Gene
Monoamine Oxidase
is
DIAGNOSES
of
Ultrasonography
is
CAUSES
of
Mutation
Hypoxia
Congenital Abnormality
Chromosome inversion
NDP gene|NDP
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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