<http://purl.obolibrary.org/obo/DOID_0060447>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An epithelial and subepithelial dystrophy that is characterized by sheet-like areas of basement membrane originating from the basal epithelial cells of the corneal epithelium and extending superficially into the epithelium."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.w3.org/2000/01/rdf-schema#label>	"epithelial basement membrane dystrophy"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Cogan corneal dystrophy"@en .
_:vb50938858	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<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_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:98956"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:H18.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060440> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-10-16T17:17:01Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060447"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<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_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"EBMD"@en .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:121820"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"microcystic corneal dystrophy"@en .
_:vb50938858	<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_0060447>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C535477"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938858	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0060447>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938858 .
_:vb50938858	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .