<http://purl.obolibrary.org/obo/DOID_0111227>	<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_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amyotrophic lateral sclerosis type 17"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A frontotemporal dementia that has_material_basis_in heterozygous mutation in CHMP2B on 3p11.2."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_9255> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasAlternativeId>	"DOID:0060208"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CHMP2B-related frontotemporal dementia"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:600795"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"FTD3"@en .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<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_0111227>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111227"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111227>	<http://www.w3.org/2000/01/rdf-schema#label>	"chromosome 3-linked frontotemporal dementia"^^<http://www.w3.org/2001/XMLSchema#string> .