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

vh8:-M8W0T5JK-9
  skos:prefLabel "mucolipidose"@fr, "mucolipidosis"@en ;
  a skos:Concept ;
  skos:narrower vh8:-HCL3BNVF-M .

vh8:-BSFBPL4W-S
  skos:prefLabel "diseases of the osteoarticular system"@en, "pathologie du système ostéoarticulaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HCL3BNVF-M .

vh8: a skos:ConceptScheme .
vh8:-HCL3BNVF-M
  skos:prefLabel "mucolipidose II"@fr, "I-cell disease"@en ;
  skos:altLabel "mucolipidosis II"@en, "maladie de Leroy-Opitz"@fr ;
  skos:inScheme vh8: ;
  skos:exactMatch <https://en.wikipedia.org/wiki/I-cell_disease> ;
  a skos:Concept ;
  skos:broader vh8:-BSFBPL4W-S, vh8:-M8W0T5JK-9 ;
  skos:definition "Inclusion-cell (I-cell) disease, also referred to as mucolipidosis II (ML II), is part of the lysosomal storage disease family and results from a defective phosphotransferase (an enzyme of the Golgi apparatus). (Wikipedia)"@en .