@prefix tsp: <http://data.loterre.fr/ark:/67375/TSP> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix isothes: <http://purl.org/iso25964/skos-thes#> .
@prefix dc11: <http://purl.org/dc/elements/1.1/> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix ns0: <http://mysite.org/> .

tsp:-PZ568JDH-8
  skos:prefLabel "mucoviscidose"@fr ;
  a skos:Concept ;
  skos:broader tsp:-S1JH7VWV-2 .

tsp: a skos:ConceptScheme .
tsp:-Pathologie
  a isothes:ConceptGroup, skos:Collection ;
  skos:prefLabel "Pathologie"@fr ;
  skos:member tsp:-S1JH7VWV-2 .

tsp:-S1JH7VWV-2
  skos:hiddenLabel "Maladie congénitale"@fr ;
  skos:narrower tsp:-PZ568JDH-8, tsp:-ZR4N0DBF-R, tsp:-FJJRBBKF-8 ;
  a skos:Concept ;
  dc11:identifier "28_19" ;
  dc:modified "2019-07-11"^^xsd:date ;
  skos:prefLabel "maladie congénitale"@fr ;
  ns0:ns0group "Pathologie"@fr ;
  skos:broader tsp:-K24VTGVC-J ;
  skos:inScheme tsp: ;
  skos:related tsp:-BBV9T59Z-S .

tsp:-BBV9T59Z-S
  skos:prefLabel "malformation"@fr ;
  a skos:Concept ;
  skos:related tsp:-S1JH7VWV-2 .

tsp:-ZR4N0DBF-R
  skos:prefLabel "hermaphrodisme"@fr ;
  a skos:Concept ;
  skos:broader tsp:-S1JH7VWV-2 .

tsp:-K24VTGVC-J
  skos:prefLabel "pathologie"@fr ;
  a skos:Concept ;
  skos:narrower tsp:-S1JH7VWV-2 .

tsp:-FJJRBBKF-8
  skos:prefLabel "aberration chromosomique"@fr ;
  a skos:Concept ;
  skos:broader tsp:-S1JH7VWV-2 .