<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110055"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50942423 .
_:vb50942423	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/2000/01/rdf-schema#label>	"amelogenesis imperfecta type 3A"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:130900"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50942423	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0111721> .
_:vb50942423	<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_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"AI3"@en .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"ADHCAI"@en .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50942423	<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_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:K00.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amelogenesis imperfecta hypomineralization type"@en .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amelogenesis imperfecta type III"@en .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"autosomal dominant amelogenesis imperfecta hypocalcification type"@en .
<http://purl.obolibrary.org/obo/DOID_0110055>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An amelogenesis imperfecta type 3 that has_material_basis_in heterozygous mutation in the FAM83H gene on chromosome 8q24."^^<http://www.w3.org/2001/XMLSchema#string> .