SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n4 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
rdfs http://www.w3.org/2000/01/rdf-schema#
obo http://www.geneontology.org/formats/oboInOwl#
rdf http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl http://www.w3.org/2002/07/owl#
xsdh http://www.w3.org/2001/XMLSchema#
Statements
Subject Item n2:DOID_0050977
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_1441
_:vb50938005
rdfs:label
spinocerebellar ataxia type 28
wdrs:describedby
n4:doid.owl
obo:id
DOID:0050977
obo:created_by
lschriml
obo:creation_date
2015-10-06T16:11:07Z
obo:hasDbXref
OMIM:610246
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, ophthalmoparesis, nystagmus and ptosis, and has_material_basis_in mutation in the AFG3L2 gene.
Subject Item _:vb50938005
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000369
wdrs:describedby
n4:doid.owl