<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50943780	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060457> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Maumenee Corneal Dystrophy"@en .
_:vb50943780	<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_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50943780 .
<http://purl.obolibrary.org/obo/DOID_0110855>	<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_0110855>	<http://www.w3.org/2000/01/rdf-schema#label>	"posterior polymorphous corneal dystrophy 1"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:H18.50"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Ched1"@en .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50943780	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50943780	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Ppcd1"@en .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0110855"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Corneal Endothelial Dystrophy 1, Autosomal Dominant"@en .
<http://purl.obolibrary.org/obo/DOID_0110855>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:122000"^^<http://www.w3.org/2001/XMLSchema#string> .