<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Viljoen-Smart syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndromic microphthalmia characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs, prognathism and intellectual disability that has_material_basis_in mutation in a region of chromosome 6q21."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C537686"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945503	<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_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MCOPS8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050739> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945503 .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.w3.org/2000/01/rdf-schema#label>	"syndromic microphthalmia 8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080636> .
_:vb50945503	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000934> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:3693"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<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_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1832440"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"syndromic microphthalmia type 8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:601349"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<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_0111803>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111803"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945503	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
_:vb50945503	<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_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:3434"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111803>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"MMEP syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .