<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_420> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:8206"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111060"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:145701"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.w3.org/2000/01/rdf-schema#label>	"Ambras type hypertrichosis universalis congenita"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:1023"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Ambras syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q84.2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"HTC1"@en .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C536605"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A hypertrichosis characterized by autosomal dominant inheritance of the presence of vellus-type hair on the entire body, especially on the face, ears and shoulders, with the exception of palms, soles, and mucous membranes that has material_basis_in chromosomal abnormalities in the region 8q22."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111060>	<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_0111060>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .