Not logged in :
Login
Facets (new session)
Description
Metadata
Settings
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:
Prader-Willi Syndrome
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
about:cgab#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
cgab
New Facet based on Instances of this Class
Attributes
Values
label
prader-willi syndrome
NEG_PART_OF
C0030705
Persons
COEXISTS_WITH
Obesity
Hyperphagia
Epilepsy
COGNITIVE DEFICIT
Rare Diseases
Reciprocal translocation
Somatotropin deficiency
Metabolic syndrome
DELETION
Thyroid Diseases
Kidney Calculi
[D]Anasarca
Neurodevelopmental disorder
Scoliosis, unspecified
Growth Disorders
Albinism
Angelman Syndrome
ASSOCIATED_WITH
Genomic Imprinting
schema:identifier
c0032897
ISA
Disease
Hereditary Diseases
Mental disorders
Mental Retardation
Syndrome
Obesity
Congenital Abnormality
Molecular Abnormality
Overweight
Congenital Disorders
Child Development Disorders
Eating Disorders
body mass
Mental deficiency
Congenital chromosomal disease
Multisystem disorder
PART_OF
C0030705
Human
Child
Adult
Females
Males
Individual
Woman
Persons
Male population group
Infant
Girls
Participant
Offspring
Infant, Newborn
Boys
sibling
Young adult
Adolescent
parent
Youth
Monozygotic twins
Child, Preschool
Toddler
Koreans (ethnic group)
Adolescents, Male
CAUSES
Disease
Obesity
Rare Diseases
Obesity, Morbid
PROCESS_OF
Human
Child
Persons
Infant
Girls
AFFECTS
C0030705
Child
Adult
Individual
Mothers
Woman
Homeostasis
Infant
Equilibrium
physiological aspects
Cousin
Young adult
Desire for food
Autistic Disorder
Metabolic Rates
Motor Development
First cousin
Genomic Imprinting
Psychomotor development
NEG_CAUSES
Angelman Syndrome
OCCURS_IN
C0030705
PRECEDES
Hyperphagia
MANIFESTATION_OF
Disease
Uniparental Disomy
NEG_MANIFESTATION_OF
Chromosome abnormality
is
LOCATION_OF
of
C0030705
Family
◂◂ First
◂ Prev
Next ▸
Last ▸▸
Page 1 of 3
Go
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
About
OpenLink Virtuoso
version 08.03.3322 as of Apr 19 2022, on Linux (x86_64-generic-linux-glibc25), Single-Server Edition (189 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software