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

vh8:-C8B6KLHH-M
  skos:prefLabel "ENT disease"@en, "pathologie ORL"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-V89H430T-7 .

vh8: a skos:ConceptScheme .
vh8:-M7X3NL2G-F
  skos:prefLabel "pathologie de la peau"@fr, "skin disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-V89H430T-7 .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-V89H430T-7 .

vh8:-V89H430T-7
  skos:definition "Shabbir syndrome (also known as laryngo–onycho–cutaneous syndrome) is a cutaneous condition inherited in an autosomal recessive fashion. It was characterized by Shabbir in 1986. It may be associated with LAMA3. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-C8B6KLHH-M, vh8:-M7X3NL2G-F, vh8:-N32K7HZ8-D ;
  skos:prefLabel "syndrome laryngo-onycho-cutané"@fr, "laryngo-onycho-cutaneous syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Laryngoonychocutaneous_syndrome> .