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Namespace Prefixes

PrefixIRI
n7https://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_0060179
rdf:type
owl:Class
rdfs:subClassOf
_:vb50938421 _:vb50938422 n2:DOID_0060309 n2:DOID_0080012
rdfs:label
Renpenning syndrome
wdrs:describedby
n7:doid.owl
obo:id
DOID:0060179
obo:created_by
lschriml
obo:creation_date
2011-11-08T03:21:30Z
obo:hasDbXref
ICD10CM:Q87.5 ORDO:3242 OMIM:309500
obo:hasExactSynonym
X-linked intellectual disability, Renpenning type Sutherland-Haan X-linked mental retardation syndrome Golabi-Ito-Hall syndrome X-linked intellectual disability due to PQBP1 mutations syndromic X-linked mental retardation 8 X-linked mental retardation with spastic diplegia X-linked mental retardation Renpenning type
obo:hasOBONamespace
disease_ontology
obo:inSubset
n5:DO_FlyBase_slim
n2:IAO_0000115
An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males.
Subject Item
_:vb50938421
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000149
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50938422
rdf:type
owl:Restriction
owl:onProperty
n2:RO_0002452
owl:someValuesFrom
n2:SYMP_0000568
wdrs:describedby
n7:doid.owl