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Namespace Prefixes

PrefixIRI
n7https://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#
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_0110958
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_1926 _:vb50943987
rdfs:label
Gaucher's disease type II
wdrs:describedby
n7:doid.owl
obo:id
DOID:0110958
obo:hasDbXref
ORDO:77260 OMIM:230900 ICD10CM:E75.2
obo:hasExactSynonym
Gaucher Disease, Acute Neuronopathic Type GD II GD2 Infantile Cerebral Gaucher Disease
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has_material_basis_in an autosomal recessive mutation of GBA on chromosome 1q22.
Subject Item
_:vb50943987
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:SO_0001537
wdrs:describedby
n7:doid.owl