@prefix jvr: <http://data.loterre.fr/ark:/67375/JVR> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix mesh: <http://id.nlm.nih.gov/mesh/vocab#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .

jvr:-Z9TSGBXH-4
  skos:prefLabel "génétique (Qualificatif)"@fr, "genetics (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-H7K65Q8S-Z
  skos:prefLabel "radiation effects (Qualifier)"@en, "effets des radiations (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-S0CS1X5R-5
  skos:prefLabel "immunology (Qualifier)"@en, "immunologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-N2WP45CN-V
  skos:prefLabel "drug effects (Qualifier)"@en, "effets des médicaments et des substances chimiques (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-B5CT14VJ-D
  skos:prefLabel "Genetic Variation"@en, "Variation génétique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-SLLQH1M2-D .

jvr:-WZF2ZR3L-B
  skos:prefLabel "physiology (Qualifier)"@en, "physiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-SLLQH1M2-D
  mesh:allowableQualifier jvr:-N2WP45CN-V, jvr:-Z9TSGBXH-4, jvr:-S0CS1X5R-5, jvr:-H7K65Q8S-Z, jvr:-WZF2ZR3L-B ;
  skos:hiddenLabel "Heteroplasmic Mutation"@en, "Macrohétéroplasmie"@fr, "Microhétéroplasmie"@fr, "Homoplasmie"@fr, "Microheteroplasmy"@en, "Macroheteroplasmy"@en, "Heteroplasmic Variation"@en, "Homoplasmy"@en, "Variation hétéroplasmique"@fr, "Mutation hétéroplasmique"@fr ;
  dc:modified "2020-06-09"^^xsd:date ;
  skos:broader jvr:-B5CT14VJ-D ;
  skos:prefLabel "Heteroplasmy"@en, "Hétéroplasmie"@fr ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D000081942> ;
  dc:created "2020-07-07"^^xsd:date ;
  dc:established "2021-01-01"^^xsd:date ;
  a skos:Concept, mesh:Descriptor ;
  skos:definition "The occurrence of more than one organellar GENOME in the organelle population of a cell, tissue, or individual organism. It is due to the accumulation of different mutations that occur within the population of individual organelles of a cell. Identical organellar GENOMES throughout a population of organelles."@en ;
  skos:inScheme jvr: .