This HTML5 document contains 28 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n3https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n5http://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
n5:DOID_0080050
rdf:type
owl:Class
rdfs:subClassOf
_:vb50940292 _:vb50940293 _:vb50940294 n5:DOID_0050737 n5:DOID_0060564 n5:DOID_0080049
rdfs:label
acromesomelic dysplasia, Maroteaux type
rdfs:comment
OMIM mapping confirmed by DO. [SN].
wdrs:describedby
n3:doid.owl
obo:id
DOID:0080050
obo:hasDbXref
ORDO:40 OMIM:602875 MESH:C535661
obo:hasOBONamespace
disease_ontology
n5:IAO_0000115
An acromesomelic dysplasia that has_material_basis_in mutation in NPR-B receptor which results_in severe dwarfism, abnormalities of the vertebral column and shortening of the limb middle and distal segments.
Subject Item
_:vb50940292
rdf:type
owl:Restriction
owl:onProperty
n5:IDO_0000664
owl:someValuesFrom
n5:GENO_0000148
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50940293
rdf:type
owl:Restriction
owl:onProperty
n5:RO_0004026
owl:someValuesFrom
n5:UBERON_0001130
wdrs:describedby
n3:doid.owl
Subject Item
_:vb50940294
rdf:type
owl:Restriction
owl:onProperty
n5:RO_0004026
owl:someValuesFrom
n5:UBERON_0002101
wdrs:describedby
n3:doid.owl