@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-BR24NLLD-X
  skos:definition "CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the Notch 3 gene on chromosome 19. The disease belongs to a family of disorders called the leukodystrophies. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-Q5X4QTZ0-T, vh8:-HMFZ2H3D-5, vh8:-N32K7HZ8-D ;
  skos:prefLabel "syndrome CADASIL"@fr, "CADASIL syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/CADASIL> .

vh8: a skos:ConceptScheme .
vh8:-Q5X4QTZ0-T
  skos:prefLabel "vascular dementia"@en, "démence vasculaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-BR24NLLD-X .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-BR24NLLD-X .

vh8:-HMFZ2H3D-5
  skos:prefLabel "pathologie des artères"@fr, "arterial disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-BR24NLLD-X .