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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)
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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:
PKD1 gene|PKD1
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An Entity of Type :
http://semmed.demo.openlinksw.com/schemas/Gene#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Semmed Gene Class
label
pkd1 gene
pkd1
sameAs
PKD1 (NIH - Gene)
PKD1
LOCATION_OF
Mutation
COEXISTS_WITH
Homologous Gene
CUX1|HCLS1|TNFRSF1B|PSIP1|SIGLEC7
ASSOCIATED_WITH
Polycystic Kidney Diseases
Polycystic Kidney, Autosomal Dominant
schema:identifier
5310
c1418599
PART_OF
Canis familiaris
Aorta
Chromosomes, Human, Pair 16
CAUSES
Disease
Polycystic Kidney, Autosomal Dominant
INTERACTS_WITH
Promoter (Genetics)
PREDISPOSES
Polycystic Kidney, Autosomal Dominant
PRODUCES
polycystic kidney disease 1 protein
is
LOCATION_OF
of
C0030705
Family
member
Individual
Population Group
Family member
Indian ethnic group
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 16
Kidney - Cortex - Renal Tubule - Collecting Duct (MMHCC)
is
PART_OF
of
Proteins
Introns
is
PROCESS_OF
of
Mutation
Splice-Site Mutation
is
AFFECTS
of
Mutation
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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