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Namespace Prefixes

PrefixIRI
n6https://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_0111794
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_9649 _:vb50945482 _:vb50945483 n2:DOID_0050736
rdfs:label
congenital nystagmus 4
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111794
obo:hasDbXref
OMIM:193003 GARD:9603
obo:hasExactSynonym
vestibulocerebellar disorder with predominant ocular signs autosomal dominant congenital nystagmus 4 NYS4
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 13q31-q33.
Subject Item
_:vb50945482
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n6:doid.owl
Subject Item
_:vb50945483
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:HP_0001197
wdrs:describedby
n6:doid.owl