This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n3https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n5http://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
n5:DOID_0111791
rdf:type
owl:Class
rdfs:subClassOf
n5:DOID_0050736 _:vb50945473 _:vb50945474 n5:DOID_9649
rdfs:label
congenital nystagmus 7
wdrs:describedby
n3:doid.owl
obo:id
DOID:0111791
obo:hasDbXref
OMIM:614826
obo:hasExactSynonym
NYS7 autosomal dominant congenital nystagmus 7
obo:hasOBONamespace
disease_ontology
n5:IAO_0000115
A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 1q31.3-q32.1.
Subject Item
_:vb50945473
rdf:type
owl:Restriction
owl:onProperty
n5:IDO_0000664
owl:someValuesFrom
n5:GENO_0000147
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50945474
rdf:type
owl:Restriction
owl:onProperty
n5:RO_0004019
owl:someValuesFrom
n5:HP_0001197
wdrs:describedby
n3:doid.owl