This HTML5 document contains 20 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n5https://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_0050719
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050718 _:vb50937456 _:vb50937457
rdfs:label
cerebral folate receptor alpha deficiency
wdrs:describedby
n5:doid.owl
obo:id
DOID:0050719
obo:created_by
lschriml
obo:creation_date
2012-06-11T02:58:59Z
obo:hasDbXref
OMIM:613068
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A vitamin metabolic disorder that has_material_basis_in mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRalpha), is located_in the brain and is characterized by progressive movement disturbance, psychomotor decline, and epilepsy.
Subject Item
_:vb50937456
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004019
owl:someValuesFrom
n2:SO_0001537
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50937457
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0004026
owl:someValuesFrom
n2:UBERON_0001893
wdrs:describedby
n5:doid.owl