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Namespace Prefixes

Prefix	IRI
n7	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_0050973

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_1441

rdfs:label

spinocerebellar ataxia type 23

wdrs:describedby

n7:doid.owl

obo:id

DOID:0050973

obo:created_by

lschriml

obo:creation_date

2015-10-06T16:11:07Z

obo:hasDbXref

OMIM:610245

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An autosomal dominnant cerebellar ataxia that is characterized by slowly progressive ataxia, dysarthria, slow saccades and hyperreflexia, has_material_basis_in mutation in the PDYN gene.