<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"chromosome 1p32-p31 deletion syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938797	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#nil> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"1p31p32 microdeletion syndrome"@en .
_:vb50938796	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50938797	<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_0060409>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060409"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938795	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938795	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50938796	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938798	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	_:vb50938797 .
_:vb50938796	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0000340> .
_:vb50938799	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938798	<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_0060409>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<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_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:Q93.5"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:613735"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#label>	"NFIA-related disorder"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938797	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	_:vb50938796 .
_:vb50938795	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938798	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	_:vb50938795 .
_:vb50938794	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938799	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50938794	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50938794	<http://www.w3.org/2002/07/owl#intersectionOf>	_:vb50938798 .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060388> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:401986"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938795	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0000159> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-09-28T17:12:14Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938799 .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938794 .
_:vb50938796	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
_:vb50938799	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0060409>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome that has_material_basis_in heterozygous mutation in the NFIA gene on chromosome 1p31 and that is characterized by macrocephaly, seizures, developmental delay, dysmorphic features, ventriculomegaly, and hypotonia."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938799	<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_0060409>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"brain malformations with or without urinary tract defects"^^<http://www.w3.org/2001/XMLSchema#string> .