<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-09-18T15:00:19Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"polydactyly, postaxial, with median cleft of upper lip"@en .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:722105002"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.w3.org/2000/01/rdf-schema#label>	"orofaciodigital syndrome V"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"OFD5"@en .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:2919"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938740	<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_0060375>	<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_0060375>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_4501> .
_:vb50938740	<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_0060375>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938740 .
<http://purl.obolibrary.org/obo/DOID_0060375>	<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_0060375>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An orofaciodigital syndrome that is characterized by postaxial polydactyly and median cleft of the upper lip and has_material_basis_in homozygous mutation in the DDX59 gene on chromosome 1q32."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938740	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:174300"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C557819"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060375"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
_:vb50938740	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1868118"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"orofaciodigital syndrome Thurston type"@en .
<http://purl.obolibrary.org/obo/DOID_0060375>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .