Facets (new session)
Description
Metadata
Settings
owl:sameAs
Inference Rule:
asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-label
virtrdf-url
None
About:
Chromosome Disorder
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NotDistinct
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An Entity of Type :
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
, within Data Space :
linked.opendata.cz
associated with source
document(s)
Type:
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
New Facet based on Instances of this Class
Attributes
Values
rdf:type
http://linked.opendata.cz/ontology/ndfrt/DiseaseOrFinding
sameAs
Chromosome Disorders
Title
Chromosome Disorders
(en)
skos:broader
Congenital Abnormalities
Genetic Diseases, Inborn
skos:prefLabel
Chromosome Disorders
(en)
adms:identifier
http://linked.opendata.cz/resource/ndfrt/disease/N0000000784/identifier/ndfrt/
http://linked.opendata.cz/resource/ndfrt/disease/N0000000784/identifier/ndfrt/N0000000784
http://linked.open...gy/ndfrt/UMLS_CUI
C0008626
skos:altLabel
Chromosomal Disorders
(en)
Chromosome Abnormality Disorders
(en)
http://linked.open.../ndfrt/SNOMED_CID
409709004
74345006
http://linked.open...gy/ndfrt/MeSH_DUI
D025063
is
skos:broader
of
Beckwith-Wiedemann Syndrome
Cri-du-Chat Syndrome
De Lange Syndrome
Down Syndrome
Prader-Willi Syndrome
Rubinstein-Taybi Syndrome
Holoprosencephaly
Angelman Syndrome
WAGR Syndrome
Williams Syndrome
Branchio-Oto-Renal Syndrome
Sex Chromosome Disorders
Silver-Russell Syndrome
Jacobsen Distal 11q Deletion Syndrome
Wolf-Hirschhorn Syndrome
Sotos Syndrome
Smith-Magenis Syndrome
22q11 Deletion Syndrome
Faceted Search & Find service v1.16.118 as of Jun 21 2024
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
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