This HTML5 document contains 12 embedded RDF statements represented using HTML+Microdata notation.

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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_0111155

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0050950

rdfs:label

autosomal recessive spinocerebellar ataxia 21

wdrs:describedby

n4:doid.owl

obo:id

DOID:0111155

obo:hasDbXref

OMIM:616719 ORDO:466794

obo:hasExactSynonym

SCAR21 autosomal recessive spinocerebellar ataxia 21 with hepatopathy acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.