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

vh8:-HWD5JP3B-D
  skos:prefLabel "nanisme"@fr, "dwarfism"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZVR7DTW1-H .

vh8: a skos:ConceptScheme .
vh8:-ZVR7DTW1-H
  skos:definition "Schwartz–Jampel syndrome (SJS) is a rare genetic disease caused by a mutation in the perlecan gene (HSPG2) which causes osteochondrodysplasia associated with myotonia. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-HWD5JP3B-D ;
  skos:prefLabel "nanisme de Schwartz-Jampel"@fr, "Schwartz-Jampel dwarfism"@en ;
  skos:altLabel "syndrome de Schwartz-Jampel"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Schwartz%E2%80%93Jampel_syndrome> .