This HTML5 document contains 23 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/
n3http://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#
n8http://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
n3:DOID_0111167
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_0080027 _:vb50944346 _:vb50944347 n3:DOID_0050737
rdfs:label
Dyggve-Melchior-Clausen disease
wdrs:describedby
n5:doid.owl
obo:id
DOID:0111167
obo:hasDbXref
OMIM:223800 GARD:6295
obo:hasExactSynonym
DMC disease pseudo-Morquio disease type I
obo:hasOBONamespace
disease_ontology
obo:inSubset
n8:DO_rare_slim
n3:IAO_0000115
A spondyloepimetaphyseal dysplasia characterized by clawed fingers, platyspondyly of the spine, abnormalities of the iliac crest, intellectual disability and mucopolysaccharide in the urine that has_material_basis_in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q21.
Subject Item
_:vb50944346
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n5:doid.owl
Subject Item
_:vb50944347
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004026
owl:someValuesFrom
n3:UBERON_0001130
wdrs:describedby
n5:doid.owl