<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"distal hereditary motor neuropathy with pyramidal features"@en .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060196"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10502"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<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_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"ALS 4"@en .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:357043"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"dHMN with upper motor neuron signs"@en .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:602433"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2014-09-16T13:49:59Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amyotrophic lateral sclerosis 4, juvenile"@en .
<http://purl.obolibrary.org/obo/DOID_0060196>	<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_0060196>	<http://www.w3.org/2000/01/rdf-schema#label>	"amyotrophic lateral sclerosis type 4"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"distal hereditary motor neuropathy with upper motor neuron signs"@en .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_332> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"emitraka"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G12.2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060196>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"amyotrophic lateral sclerosis 4"@en .