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Namespace Prefixes

PrefixIRI
n8https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n4http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_10241
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_583 n2:DOID_0050737 _:vb50946784
rdfs:label
thalassemia
rdfs:comment
OMIM mapping confirmed by DO. [LS].
wdrs:describedby
n8:doid.owl
obo:id
DOID:10241
obo:hasAlternativeId
DOID:12242 DOID:12243
obo:hasDbXref
UMLS_CUI:C0039730 SNOMEDCT_US_2021_09_01:191192008 ICD9CM:282.4 MESH:D013789 ICD10CM:D56 NCI:C35069 GARD:7756
obo:hasExactSynonym
thalassemia Hb-S disease with crisis Sickle-cell thalassemia without crisis thalassemia Hb-S disease without crisis Sickle-cell thalassemia with crisis
obo:hasOBONamespace
disease_ontology
obo:inSubset
n4:NCIthesaurus
n2:IAO_0000115
A hemolytic anemia characterized by decreased synthesis of one or more hemoglobin polypeptide chains.
Subject Item
_:vb50946784
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n8:doid.owl