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

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JL0VPXFQ-6 .

vh8:-VMQGBJL5-L
  skos:prefLabel "tumeur bénigne"@fr, "benign neoplasm"@en ;
  a skos:Concept ;
  skos:narrower vh8:-JL0VPXFQ-6 .

vh8:-CCS31G12-M
  skos:prefLabel "endocrinopathy"@en, "endocrinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JL0VPXFQ-6 .

vh8:-JL0VPXFQ-6
  skos:broader vh8:-VMQGBJL5-L, vh8:-N32K7HZ8-D, vh8:-CCS31G12-M ;
  a skos:Concept ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Multiple_endocrine_neoplasia_type_1>, <https://fr.wikipedia.org/wiki/N%C3%A9oplasie_endocrinienne_multiple_type_1> ;
  skos:prefLabel "polyadénomatose endocrinienne de type I"@fr, "multiple endocrine neoplasia type I"@en ;
  skos:definition "Multiple endocrine neoplasia type 1 (MEN-1) is one of a group of disorders, the multiple endocrine neoplasias, that affect the endocrine system through development of neoplastic lesions in pituitary, parathyroid gland and pancreas. (Wikipedia)"@en, "La néoplasie endocrinienne multiple type 1 ou NEM1 ou syndrome de Wermer est une maladie génétique impliquant plus de 20 tumeurs endocrines et non-endocrines. (Wikipédia)"@fr ;
  skos:inScheme vh8: .