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Description
Metadata
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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
Inverse Functional Properties:
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects
"Same As":
Disabled (fastest)
Apply to subjects only
Apply to objects only
Apply to both subjects and objects (recommended)
Apply to subjects, objects and predicates (not recommended on big datasets)
Apply to predicates only (special use cases only)
About:
ADGRV1
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Sponge
NotDistinct
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An Entity of Type :
semmed:Gene
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
label
adgrv1
LOCATION_OF
Protein Expression
natural genetic mutation
ASSOCIATED_WITH
Epilepsy
schema:identifier
84059
PART_OF
C0030705
Muscle
Mus
sibling
Chromosomes, Human, Pair 13
CAUSES
Usher Syndromes
Deafness
INTERACTS_WITH
Binding Sites
AFFECTS
Epilepsies, Myoclonic
Eyelash
compared_with
USH2A
PREDISPOSES
Epilepsy
is
LOCATION_OF
of
Family
cohort
sibling
Mice, Inbred CBA
HCT116 Cells
is
COEXISTS_WITH
of
Homologous Gene
22q11.2
seven-transmembrane G-protein-coupled receptor
is
PART_OF
of
Introns
is
PROCESS_OF
of
Mutation
Gene Mutation
Mutation, Missense
natural genetic mutation
is
PRODUCES
of
USH2A
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
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