This HTML5 document contains 23 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n5https://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#
n8http://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_0080523
rdf:type
owl:Class
rdfs:subClassOf
_:vb50941089 _:vb50941090 n2:DOID_0050736 n2:DOID_10579
rdfs:label
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
wdrs:describedby
n5:doid.owl
obo:id
DOID:0080523
obo:hasDbXref
ORDO:313808 OMIM:221820 GARD:10981
obo:hasExactSynonym
hereditary diffuse leukoencephalopathy with spheroids
obo:hasOBONamespace
disease_ontology
obo:inSubset
n8:DO_rare_slim
n2:IAO_0000115
A leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has_material_basis_in heterozygous mutation in the CSF1R gene on chromosome 5q32.
Subject Item
_:vb50941089
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50941090
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002488
owl:someValuesFrom
n2:HP_0003581
wdrs:describedby
n5:doid.owl