<http://purl.obolibrary.org/obo/DOID_0050539>	<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_0050539>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:64746"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050539"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary motor and sensory neuropathy Guadalajara neuronal type"@en .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0392553"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary motor and sensory neuropathy type 2"@en .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.w3.org/2000/01/rdf-schema#label>	"Charcot-Marie-Tooth disease type 2"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:356.0"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<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_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:118230"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:12431"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_10595> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:604484"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Xref MGI.\nOMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary motor and sensory neuropathy Okinawa type"@en .
<http://purl.obolibrary.org/obo/DOID_0050539>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:193158000"^^<http://www.w3.org/2001/XMLSchema#string> .