<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0751587"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<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_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:PS125310"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hereditary multi-infarct dementia"@en .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:13945"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:600142"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84606"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:I67.850"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy"@en .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:136"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:1049"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D046589"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_10579> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:390723008"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.w3.org/2000/01/rdf-schema#label>	"CADASIL"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_13945>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .