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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-eturtle-containers
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virtrdf-ifp
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virtrdf-meta-entity-class
None
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"Same As":
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Apply to subjects only
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Apply to both subjects and objects (recommended)
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About:
DVL3 gene|DVL3
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An Entity of Type :
about:c1414202#this
, within Data Space :
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Attributes
Values
type
Semmed Gene Class
DVL3 gene|DVL3
label
DVL3 gene|DVL3
dvl3
dvl3 gene
sameAs
DVL3
DVL3 (NIH - Gene)
terms:part_of
Chromosomes, Human, Pair 16
terms:causes
Robinow syndrome
terms:location_of
Mutation
Loss of Heterozygosity
LOCATION_OF
Mutation
schema:identifier
1857
C1414202|1857
c1414202
CAUSES
Robinow syndrome
is
type
of
DVL3 gene|DVL3
is
terms:location_of
of
Stem cells
is
terms:coexists_with
of
CELSR1 gene|CELSR1
SCRIB gene|SCRIB
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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Microdata
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