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

vh8:-P22G5PPZ-K
  skos:prefLabel "sclerocornea"@en, "sclérocornée"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-CQWDC3HQ-X .

vh8:-MBLSJ4C4-D
  skos:prefLabel "microphtalmie"@fr, "microphthalmia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CQWDC3HQ-X .

vh8: a skos:ConceptScheme .
vh8:-CQWDC3HQ-X
  skos:broader vh8:-MBLSJ4C4-D, vh8:-P22G5PPZ-K, vh8:-N32K7HZ8-D, vh8:-KRM787H0-5 ;
  skos:altLabel "syndrome MLS"@fr, "MLS syndrome"@en, "microphthalmia with linear skin defects"@en, "microphtalmie, aplasie dermique et sclérocornée"@fr, "microphtalmie avec défauts linéaires cutanés"@fr ;
  a skos:Concept ;
  skos:prefLabel "syndrome de MIDAS"@fr, "MIDAS syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Microphthalmia%E2%80%93dermal_aplasia%E2%80%93sclerocornea_syndrome> ;
  skos:definition "Microphthalmia–dermal aplasia–sclerocornea syndrome is a condition characterized by linear skin lesions. (Wikipedia)"@en ;
  skos:inScheme vh8: .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-CQWDC3HQ-X .

vh8:-KRM787H0-5
  skos:prefLabel "aplasie cutanée congénitale"@fr, "aplasia cutis congenita"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CQWDC3HQ-X .