<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060379> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C2931762"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<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_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C538182"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:720419000"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060384"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:1786"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Opitz Mollica Sorge syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060384>	<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_0060384>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:101805"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-09-21T15:34:09Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Opitz-Caltabiano syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:494"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An acrofacial dysostosis that is characterized by intrauterine growth retardation, short stature, microcephaly, cleft palate, limb hypoplasia, simian creases and cryptorchidism/hypospadias."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060384>	<http://www.w3.org/2000/01/rdf-schema#label>	"acrofacial dysostosis, Catania type"^^<http://www.w3.org/2001/XMLSchema#string> .