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

vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T33HR75Z-G .

vh8:-S8V26HKD-C
  skos:prefLabel "pathologie des phanères"@fr, "skin appendages disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-T33HR75Z-G .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T33HR75Z-G .

vh8:-T33HR75Z-G
  skos:exactMatch <https://en.wikipedia.org/wiki/Trichothiodystrophy>, <https://fr.wikipedia.org/wiki/Trichothiodystrophie> ;
  skos:broader vh8:-PLFNN4S2-4, vh8:-N32K7HZ8-D, vh8:-S8V26HKD-C ;
  skos:prefLabel "trichothiodystrophy"@en, "trichothiodystrophie"@fr ;
  a skos:Concept ;
  skos:definition "Trichothiodystrophy (TTD) is an autosomal recessive inherited disorder characterised by brittle hair and intellectual impairment. (Wikipedia)"@en, "La Trichothiodystrophie ou TTD est un groupe hétérogène de maladies génétiques rares. (Wikipédia)"@fr ;
  skos:inScheme vh8: .