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

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-XS1XJPNX-C .

vh8: a skos:ConceptScheme .
vh8:-XS1XJPNX-C
  skos:broader vh8:-RFF18FW6-W, vh8:-N32K7HZ8-D ;
  skos:prefLabel "kératodermie palmoplantaire de Papillon-Lefèvre"@fr, "Papillon-Lefèvre's syndrome"@en ;
  skos:inScheme vh8: ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Papillon%E2%80%93Lef%C3%A8vre_syndrome> ;
  skos:altLabel "syndrome de Papillon-Lefèvre"@fr, "maladie de Papillon-Lefèvre"@fr, "palmoplantar keratoderma with periodontitis"@en ;
  a skos:Concept ;
  skos:definition "Papillon–Lefèvre syndrome (PLS), also known as palmoplantar keratoderma with periodontitis, is an autosomal recessive genetic disorder caused by a deficiency in cathepsin C. (Wikipedia)"@en .

vh8:-RFF18FW6-W
  skos:prefLabel "kératodermie"@fr, "keratoderma"@en ;
  a skos:Concept ;
  skos:narrower vh8:-XS1XJPNX-C .