This HTML5 document contains 21 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_0110058
- rdf:type
-
owl:Class
- rdfs:subClassOf
-
n2:DOID_0080009
_:vb50942429
n2:DOID_2187
- rdfs:label
-
amelogenesis imperfecta type 1E
- wdrs:describedby
-
n6:doid.owl
- obo:id
-
DOID:0110058
- obo:hasDbXref
-
ICD10CM:K00.5
OMIM:301200
- obo:hasExactSynonym
-
amelogenesis imperfecta type IE
AIH1
amelogenesis imperfecta hypomaturationtype with snow-capped teeth
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
X-linked amelogenesis imperfecta 1
- obo:hasOBONamespace
-
disease_ontology
- obo:hasRelatedSynonym
-
X-linked enamel hypoplasia
- n2:IAO_0000115
-
An amelogenesis imperfecta that has_material_basis_in X-linked dominant mutation in the gene encoding amelogenin (AMELX).
- Subject Item
- _:vb50942429
- rdf:type
-
owl:Restriction
- owl:onProperty
-
n2:IDO_0000664
- owl:someValuesFrom
-
n2:GENO_0000146
- wdrs:describedby
-
n6:doid.owl