<http://purl.obolibrary.org/obo/DOID_0111673>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A bone development disease characterized by early developmental delay primarily involving speech, distinct facial features, short stature, brachydactyly, clubfoot deformities, cataracts, and microcephaly that has_material_basis_in heterozygous mutation in COG4 on chromosome 16q22.1."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111673"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"microcephalic osteodysplastic dysplasia, Saul-Wilson type"@en .
_:vb50945250	<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_0111673>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50945250	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:85172"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1300285"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"SWILS"@en .
<http://purl.obolibrary.org/obo/DOID_0111673>	<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_0111673>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0080006> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:389197004"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:618150"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50945250 .
<http://purl.obolibrary.org/obo/DOID_0111673>	<http://www.w3.org/2000/01/rdf-schema#label>	"Saul-Wilson syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50945250	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50945250	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .