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

vh8:-RSBS7B77-7
  skos:prefLabel "coagulopathy"@en, "coagulopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JVL4WG1X-L .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-JVL4WG1X-L .

vh8: a skos:ConceptScheme .
vh8:-JVL4WG1X-L
  skos:exactMatch <https://fr.wikipedia.org/wiki/D%C3%A9ficit_en_prot%C3%A9ine_C>, <https://www.wikidata.org/wiki/Q1504570>, <https://en.wikipedia.org/wiki/Protein_C_deficiency> ;
  skos:prefLabel "déficit en protéine C"@fr, "protein C deficiency"@en ;
  a skos:Concept ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-RSBS7B77-7 ;
  skos:definition "Protein C deficiency is a rare genetic trait that predisposes to thrombotic disease. It was first described in 1981. The disease belongs to a group of genetic disorders known as thrombophilias. (Wikipedia)"@en, "Le déficit en protéine C est une maladie génétique rare source de thrombophilie (risque de thromboses). (Wikipédia)"@fr ;
  skos:inScheme vh8: .