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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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Apply to subjects only
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Apply to both subjects and objects (recommended)
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About:
7q11.23
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about:nusq#this
, within Data Space :
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associated with source
document(s)
Type:
nusq
New Facet based on Instances of this Class
Attributes
Values
label
7q11.23
NEG_LOCATION_OF
Williams Syndrome
LOCATION_OF
Disease
Hereditary Diseases
Epilepsy
Rare Diseases
Williams Syndrome
Child Development Disorders
Neurodevelopmental disorder
Multisystem disorder
Eosinophilic cellulitis
COEXISTS_WITH
SCTR gene|SCTR
7q22.1
ASSOCIATED_WITH
Williams Syndrome
Cholangiocarcinoma
Autism spectrum disorder
schema:identifier
c1521638
PART_OF
C0030705
CAUSES
Williams Syndrome
INTERACTS_WITH
Elastin|ELN
is
LOCATION_OF
of
C0030705
is
COEXISTS_WITH
of
Genes
Candidate Disease Gene
CDKN1C gene|CDKN1C
4p16.3
is
PART_OF
of
Genes
DNA Sequence
EIF4H
is
INTERACTS_WITH
of
ELN gene|ELN
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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