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

vh8:-BGHF6WV3-R
  skos:prefLabel "polyadénomatose endocrinienne de type II"@fr, "multiple endocrine neoplasia type II"@en ;
  skos:definition "Multiple endocrine neoplasia type 2 (also known as \"Pheochromocytoma and amyloid producing medullary thyroid carcinoma\",[1] \"PTC syndrome,\"[1] and \"Sipple syndrome\"[1]) is a group of medical disorders associated with tumors of the endocrine system. (Wikipedia)"@en, "La néoplasie endocrinienne multiple de type 2 est la forme héréditaire du cancer médullaire de la thyroïde. Il existe trois sous types en fonction de l'association des cancers endocriniens. (Wikipédia)"@fr ;
  skos:inScheme vh8: ;
  a skos:Concept ;
  skos:broader vh8:-T4XJ4RLD-P, vh8:-CCS31G12-M, vh8:-N32K7HZ8-D ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Multiple_endocrine_neoplasia_type_2>, <https://fr.wikipedia.org/wiki/N%C3%A9oplasie_endocrinienne_multiple#N%C3%A9oplasie_endocrinienne_multiple_de_type_2> .

vh8: a skos:ConceptScheme .
vh8:-T4XJ4RLD-P
  skos:prefLabel "cancer"@fr, "cancer"@en ;
  a skos:Concept ;
  skos:narrower vh8:-BGHF6WV3-R .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-BGHF6WV3-R .

vh8:-CCS31G12-M
  skos:prefLabel "endocrinopathy"@en, "endocrinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-BGHF6WV3-R .