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owl:sameAs
Inference Rule:
asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-label
virtrdf-url
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About:
Blood Coagulation Disorders, Inherited
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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
Title
Blood Coagulation Disorders, Inherited
(en)
skos:broader
Blood Coagulation Disorders
Genetic Diseases, Inborn
skos:prefLabel
Blood Coagulation Disorders, Inherited
(en)
adms:identifier
http://linked.opendata.cz/resource/ndfrt/disease/N0000010965/identifier/ndfrt/N0000010965
http://linked.opendata.cz/resource/ndfrt/disease/N0000010965/identifier/ndfrt/
http://linked.open...gy/ndfrt/UMLS_CUI
C0852077
skos:altLabel
Coagulation Disorders, Inherited
(en)
Hereditary Blood Coagulation Disorders
(en)
Hereditary Coagulation Disorders
(en)
Inherited Blood Coagulation Disorders
(en)
Inherited Coagulation Disorders
(en)
http://linked.open...gy/ndfrt/MeSH_DUI
D025861
is
skos:broader
of
Afibrinogenemia
Bernard-Soulier Syndrome
Hemophilia B
Factor V Deficiency
Factor VII Deficiency
Factor X Deficiency
Factor XI Deficiency
Factor XII Deficiency
Factor XIII Deficiency
Hemophilia A
Hypoprothrombinemias
Thrombasthenia
von Willebrand Diseases
Wiskott-Aldrich Syndrome
Activated Protein C Resistance
Protein C Deficiency
Antithrombin III Deficiency
Hermanski-Pudlak Syndrome
Gray Platelet Syndrome
Faceted Search & Find service v1.16.118 as of Jun 21 2024
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