<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Moebius congenital oculofacial paralysis"@en .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:8549"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50949046	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50949046	<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_13501>	<http://www.w3.org/2000/01/rdf-schema#label>	"Mobius syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_1756> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Oromandibular-limb hypogenesis spectrum"@en .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:89444000"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50949046	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000094> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D020331"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:13501"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<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_13501>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:157900"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s)."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<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_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q87.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50949046 .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0221060"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50949046	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_13501>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84893"^^<http://www.w3.org/2001/XMLSchema#string> .