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Namespace Prefixes

PrefixIRI
n7https://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#
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_0060638
rdf:type
owl:Class
rdfs:subClassOf
n3:DOID_11717 n3:DOID_0080015 n3:DOID_655 n3:DOID_0050737 _:vb50939136 _:vb50939135
rdfs:label
neonatal diabetes mellitus with congenital hypothyroidism
wdrs:describedby
n7:doid.owl
obo:id
DOID:0060638
obo:hasDbXref
ORDO:79118 OMIM:610199
obo:hasExactSynonym
NDH syndrome
obo:hasOBONamespace
disease_ontology
n3:IAO_0000115
A neonatal diabetes that is characterized by intrauterine growth retardation, hypothyroidism and onset of nonimmune diabetes mellitus within the first few weeks of life, and that has_material_basis_in homozygous or compound heterozygous mutations in the GLIS3 gene on chromosome 9p24.
Subject Item
_:vb50939135
rdf:type
owl:Restriction
owl:onProperty
n3:IDO_0000664
owl:someValuesFrom
n3:GENO_0000148
wdrs:describedby
n7:doid.owl
Subject Item
_:vb50939136
rdf:type
owl:Restriction
owl:onProperty
n3:RO_0004019
owl:someValuesFrom
n3:HP_0001197
wdrs:describedby
n7:doid.owl