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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_0112013
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050736 n2:DOID_0112011 _:vb50945916
rdfs:label
autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques
wdrs:describedby
n5:doid.owl
obo:id
DOID:0112013
obo:hasDbXref
OMIM:614594
obo:hasExactSynonym
Olmsted syndrome 1 autosomal dominant Olmsted syndrome OLMS1
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in heterozygous mutation in TRPV3 on chromosome 17p13.2.
Subject Item
_:vb50945916
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n5:doid.owl