<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:11974"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060388> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 3q29 region."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.w3.org/2000/01/rdf-schema#label>	"chromosome 3q29 microdeletion syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C567184"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<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_0060419>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:609425"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"3qter deletion"@en .
<http://purl.obolibrary.org/obo/DOID_0060419>	<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_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:65286"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"3q29 microdeletion syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"3q29 recurrent deletion"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-09-28T17:45:50Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"3q subtelomere deletion syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_0060419>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060419"^^<http://www.w3.org/2001/XMLSchema#string> .