This HTML5 document contains 28 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n13http://en.wikipedia.org/wiki/List_of_diseases_(H)
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
n4http://en.wikipedia.org/wiki/Category:
n6http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n12http://caligraph.org/ontology/MeSH_code_(C16)
owlhttp://www.w3.org/2002/07/owl#
clgohttp://caligraph.org/ontology/
n5http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
dbrhttp://dbpedia.org/resource/
clgrhttp://caligraph.org/resource/
Subject Item
clgr:Hereditary_elliptocytosis
rdf:type
clgo:Hereditary_hemolytic_anemia owl:NamedIndividual clgo:Autosomal_dominant_disorder n12:
rdfs:label
Hereditary elliptocytosis
owl:sameAs
dbr:Hereditary_elliptocytosis
prov:wasDerivedFrom
n4:Hereditary_hemolytic_anemias n5:Congenital_hemolytic_anemia n5:Neonatal_jaundice n6: n5:Hereditary_elliptocytosis n5:Asymptomatic n5:Elliptocyte n4:Autosomal_dominant_disorders n5:Anemia n13: n5:Hematologic_disease
skos:prefLabel
Hereditary elliptocytosis
skos:altLabel
hereditary elliptocytosis elliptocytosis
clgo:diseasesDB
4172
clgo:eMedicineSubject
ped
clgo:eMedicineTopic
987
clgo:icd10
D58.1
clgo:icd9
282.1
clgo:medlinePlus
000563
clgo:meshId
D004612
clgo:omim
611804