This HTML5 document contains 27 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n8https://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#
n5http://purl.obolibrary.org/obo/doid#
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_0050883
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_1289 _:vb50937782 n2:DOID_0050737
rdfs:label
infantile cerebellar-retinal degeneration
wdrs:describedby
n8:doid.owl
obo:id
DOID:0050883
obo:created_by
lschriml
obo:creation_date
2014-08-06T04:09:42Z
obo:hasDbXref
OMIM:614559 GARD:13264
obo:hasOBONamespace
disease_ontology
obo:inSubset
n5:DO_FlyBase_slim
n2:IAO_0000115
A neurodegenerative disease that is characterized by onset between ages 2 and 6 months of truncal hypotonia, athetosis, seizures, and ophthalmologic abnormalities, particularly optic atrophy and retinal degeneration.
Subject Item
_:vb50937782
rdf:type
owl:Class
owl:intersectionOf
_:vb50937785
wdrs:describedby
n8:doid.owl
Subject Item
_:vb50937783
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n8:doid.owl
Subject Item
_:vb50937784
rdf:first
_:vb50937783
rdf:rest
rdf:nil
wdrs:describedby
n8:doid.owl
Subject Item
_:vb50937785
rdf:first
n2:DOID_4
rdf:rest
_:vb50937784
wdrs:describedby
n8:doid.owl