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:
Hereditary Hemolytic Anemia
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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
Anemia, Hemolytic, Congenital
Title
Anemia, Hemolytic, Congenital
(en)
skos:broader
Anemia, Hemolytic
Genetic Diseases, Inborn
skos:prefLabel
Anemia, Hemolytic, Congenital
(en)
adms:identifier
http://linked.opendata.cz/resource/ndfrt/disease/N0000000389/identifier/ndfrt/
http://linked.opendata.cz/resource/ndfrt/disease/N0000000389/identifier/ndfrt/N0000000389
http://linked.open...gy/ndfrt/UMLS_CUI
C0002881
skos:altLabel
Anemia, Hemolytic, Hereditary
(en)
Congenital Hemolytic Anemia
(en)
Hemolytic Anemia, Congenital
(en)
Hemolytic Anemia, Hereditary
(en)
Hereditary Hemolytic Anemia
(en)
http://linked.open.../ndfrt/SNOMED_CID
38911009
42601008
http://linked.open...gy/ndfrt/MeSH_DUI
D000745
is
skos:broader
of
Anemia, Dyserythropoietic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Sickle Cell
Elliptocytosis, Hereditary
Glucosephosphate Dehydrogenase Deficiency
Hemoglobin C Disease
Spherocytosis, Hereditary
Thalassemia
Faceted Search & Find service v1.16.118 as of Jun 21 2024
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