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

vh8:-MF063W02-Q
  skos:exactMatch <https://en.wikipedia.org/wiki/COACH_syndrome> ;
  skos:broader vh8:-C0CS7VBM-F, vh8:-NZTTV47J-G, vh8:-GTW24CC0-J, vh8:-F0Q8HP18-R, vh8:-QG1RVCT9-L ;
  a skos:Concept ;
  skos:definition "COACH syndrome is a rare recessive genetic disease. The name is an acronym of the defining signs: cerebellar vermis aplasia, oligophrenia, congenital ataxia, coloboma and hepatic fibrosis. (Wikipedia)"@en ;
  skos:prefLabel "syndrome COACH"@fr, "COACH syndrome"@en ;
  skos:inScheme vh8: .

vh8:-C0CS7VBM-F
  skos:prefLabel "pathologie de l'oeil"@fr, "eye disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MF063W02-Q .

vh8:-F0Q8HP18-R
  skos:prefLabel "malformation"@fr, "malformation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MF063W02-Q .

vh8: a skos:ConceptScheme .
vh8:-NZTTV47J-G
  skos:prefLabel "hepatic disease"@en, "pathologie du foie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-MF063W02-Q .

vh8:-GTW24CC0-J
  skos:prefLabel "pathologie du cervelet"@fr, "cerebellar disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-MF063W02-Q .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-MF063W02-Q .