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Namespace Prefixes

PrefixIRI
n6https://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_0111664
rdf:type
owl:Class
rdfs:subClassOf
_:vb50945235 n2:DOID_14793 n2:DOID_0080012
rdfs:label
ectodermal dysplasia 1
wdrs:describedby
n6:doid.owl
obo:id
DOID:0111664
obo:hasDbXref
SNOMEDCT_US_2021_09_01:239007005 OMIM:305100 ORDO:181 NCI:C84562 MESH:D053358 UMLS_CUI:C0162359
obo:hasExactSynonym
hypohidrotic ectodermal dysplasia, X-Linked CST syndrome ectodermal dysplasia 1, hypohidrotic, X-linked ED1 X-linked anhidrotic ectodermal dysplasia HED1 XHED XLHED Christ-Siemens-Touraine syndrome ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked ectodermal dysplasia 1, anhidrotic
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A hypohidrotic ectodermal dysplasia that has_material_basis_in X-linked recessive mutation in EDA on chromosome Xq13.1.
Subject Item
_:vb50945235
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000149
wdrs:describedby
n6:doid.owl