<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:104500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/2000/01/rdf-schema#label>	"amelogenesis imperfecta type 1B"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_2187> .
_:vb50942417	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
_:vb50942417	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary localized enamel hypoplasia"@en .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50942417 .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"AIH2"@en .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amelogenesis imperfecta type IB"@en .
_:vb50942417	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"AI1B"@en .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant hypoplastic local amelogenesis imperfecta"@en .
_:vb50942417	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110052"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:K00.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110052>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13."^^<http://www.w3.org/2001/XMLSchema#string> .