This HTML5 document contains 30 embedded RDF statements represented using HTML+Microdata notation.
The embedded RDF content will be recognized by any processor of HTML5 Microdata.
Namespace Prefixes
Prefix | IRI |
n6 | https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/ |
n2 | http://purl.obolibrary.org/obo/ |
wdrs | http://www.w3.org/2007/05/powder-s# |
rdfs | http://www.w3.org/2000/01/rdf-schema# |
obo | http://www.geneontology.org/formats/oboInOwl# |
rdf | http://www.w3.org/1999/02/22-rdf-syntax-ns# |
owl | http://www.w3.org/2002/07/owl# |
xsdh | http://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