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:
Amino Acid Metabolism Disorder
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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
Amino Acid Metabolism, Inborn Errors
Title
Amino Acid Metabolism, Inborn Errors
(en)
skos:broader
Metabolism, Inborn Errors
skos:prefLabel
Amino Acid Metabolism, Inborn Errors
(en)
adms:identifier
http://linked.opendata.cz/resource/ndfrt/disease/N0000000369/identifier/ndfrt/N0000000369
http://linked.opendata.cz/resource/ndfrt/disease/N0000000369/identifier/ndfrt/
http://linked.open...gy/ndfrt/UMLS_CUI
C0002514
skos:altLabel
Amino Acid Metabolism Disorders, Inborn
(en)
Amino Acid Metabolism, Inborn Error
(en)
Amino Acidopathies, Congenital
(en)
Amino Acidopathies, Inborn
(en)
Congenital Amino Acidopathies
(en)
Inborn Errors, Amino Acid Metabolism
(en)
http://linked.open.../ndfrt/SNOMED_CID
190680002
42930003
44779003
http://linked.open...gy/ndfrt/MeSH_DUI
D000592
is
skos:broader
of
Albinism
Alkaptonuria
Maple Syrup Urine Disease
Multiple Carboxylase Deficiency
Phenylketonurias
Hyperhomocysteinemia
Hyperglycinemia, Nonketotic
Hyperlysinemias
Tyrosinemias
Urea Cycle Disorders, Inborn
Prolidase Deficiency
Propionic Acidemia
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Faceted Search & Find service v1.16.118 as of Jun 21 2024
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