@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 owl: <http://www.w3.org/2002/07/owl#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

jvr:-WWJHCQRB-K
  skos:prefLabel "surgery (Qualifier)"@en, "chirurgie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDXQ5280-F
  skos:prefLabel "mortality (Qualifier)"@en, "mortalité (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-HPKB70N8-W
  skos:prefLabel "rehabilitation (Qualifier)"@en, "rééducation et réadaptation (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-VG20R78F-K
  skos:prefLabel "embryologie (Qualificatif)"@fr, "embryology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-PJ9KTHCL-G
  skos:prefLabel "Metabolism, Inborn Errors"@en, "Erreurs innées du métabolisme"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-MQ2BL28X-C .

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

jvr:-MQ2BL28X-C
  skos:altLabel "Trouble péroxysomial"@fr, "Maladies péroxysomales"@fr, "Trouble péroxysomal"@fr, "Troubles péroxysomiaux"@fr, "Troubles péroxysomaux"@fr ;
  skos:hiddenLabel "Peroxisomal Dysfunction, General"@en, "Hyperpipecolic Acidemia"@en, "Adrénoleucodystrophie néonatale"@fr, "Adrenoleukodystrophy, Autosomal, Neonatal Form"@en, "Maladie péroxisomiale à déficits enzymatiques multiples"@fr, "Maladie péroxisomiale à déficit enzymatique unique"@fr, "Neonatal Adrenoleukodystrophy"@en, "Maladie péroxisomale à déficit enzymatique généralisé"@fr, "Maladie péroxisomiale à déficit enzymatique généralisé"@fr, "Hyperpipécolatémie"@fr, "Maladie péroxisomale à déficits enzymatiques multiples"@fr, "Hyperpipecolatemia"@en, "Peroxisomal Dysfunction, Multiple"@en, "Acidémie pipécolique"@fr, "Adrenoleukodystrophy, Neonatal"@en, "Maladie péroxisomale à déficit enzymatique unique"@fr, "Peroxisomal Dysfunction, Single"@en, "Adrenoleukodystrophy, Autosomal Neonatal Form"@en ;
  mesh:allowableQualifier jvr:-NHL3D2X0-S, jvr:-XV06LPML-W, jvr:-MDQBX560-1, jvr:-T6JZ48ZV-N, jvr:-Z9TSGBXH-4, jvr:-SDPG013V-D, jvr:-KRXG97RR-5, jvr:-J9Z93VFN-9, jvr:-WWJHCQRB-K, jvr:-B6C87218-T, jvr:-CSKTXWF5-F, jvr:-SBNWSM1T-R, jvr:-W6T67RP3-2, jvr:-S0CS1X5R-5, jvr:-DH7H9MJ2-N, jvr:-RC3PND0F-S, jvr:-BT300B3G-Q, jvr:-WQ00QWRG-J, jvr:-T1QJHLQ4-J, jvr:-JVKFK2NX-2, jvr:-GXVR9QN8-P, jvr:-XVHTZRCG-7, jvr:-CB30NGKB-3, jvr:-SDXQ5280-F, jvr:-W4X1LN61-R, jvr:-HPKB70N8-W, jvr:-L6C0XPHT-4, jvr:-BBD0S71C-R, jvr:-P1X8SCQ6-K, jvr:-KFM33PF8-L, jvr:-BQ3W1P91-F, jvr:-ZJBZVRWR-8, jvr:-W6SQV79N-S, jvr:-VG20R78F-K ;
  skos:broader jvr:-PJ9KTHCL-G ;
  skos:narrower jvr:-HM541ZMH-6, jvr:-SST3MBRR-Z, jvr:-SS1XPWM3-C, jvr:-VQ7DWFHZ-Z, jvr:-QSV8SCLW-L, jvr:-MHKLJX03-S, jvr:-SHBQS9GT-G ;
  skos:definition "A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders."@en ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D018901> ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-D7ZX09M4-S ;
  dc:established "1996-01-01"^^xsd:date ;
  skos:prefLabel "Maladies péroxysomiales"@fr, "Peroxisomal Disorders"@en ;
  skos:inScheme jvr: ;
  dc:created "1994-12-27"^^xsd:date ;
  dc:modified "2015-06-08"^^xsd:date .

jvr:-L6C0XPHT-4
  skos:prefLabel "métabolisme (Qualificatif)"@fr, "metabolism (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-WQ00QWRG-J
  skos:prefLabel "physiopathologie (Qualificatif)"@fr, "physiopathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-DH7H9MJ2-N
  skos:prefLabel "anatomopathologie (Qualificatif)"@fr, "pathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-MDQBX560-1
  skos:prefLabel "radiotherapy (Qualifier)"@en, "radiothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-ZJBZVRWR-8
  skos:prefLabel "parasitologie (Qualificatif)"@fr, "parasitology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6T67RP3-2
  skos:prefLabel "diagnostic imaging (Qualifier)"@en, "imagerie diagnostique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-B6C87218-T
  skos:prefLabel "prévention et contrôle (Qualificatif)"@fr, "prevention & control (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SST3MBRR-Z
  skos:prefLabel "Chondrodysplasia Punctata, Rhizomelic"@en, "Chondrodysplasie ponctuée rhizomélique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr:-BQ3W1P91-F
  skos:prefLabel "thérapie (Qualificatif)"@fr, "therapy (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-KRXG97RR-5
  skos:prefLabel "diagnostic (Qualificatif)"@fr, "diagnosis (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-J9Z93VFN-9
  skos:prefLabel "enzymology (Qualifier)"@en, "enzymologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-QSV8SCLW-L
  skos:prefLabel "Refsum Disease, Infantile"@en, "Maladie de Refsum infantile"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr:-T1QJHLQ4-J
  skos:prefLabel "microbiology (Qualifier)"@en, "microbiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-MHKLJX03-S
  skos:prefLabel "Refsum Disease"@en, "Maladie de Refsum"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr:-KFM33PF8-L
  skos:prefLabel "médecine vétérinaire (Qualificatif)"@fr, "veterinary (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SHBQS9GT-G
  skos:prefLabel "Acatalasie"@fr, "Acatalasia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr: a skos:ConceptScheme .
jvr:-BBD0S71C-R
  skos:prefLabel "induit chimiquement (Qualificatif)"@fr, "chemically induced (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-XVHTZRCG-7
  skos:prefLabel "étiologie (Qualificatif)"@fr, "etiology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDPG013V-D
  skos:prefLabel "psychology (Qualifier)"@en, "psychologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-P1X8SCQ6-K
  skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-T6JZ48ZV-N
  skos:prefLabel "complications (Qualifier)"@en, "complications (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6SQV79N-S
  skos:prefLabel "classification (Qualifier)"@en, "classification (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-GXVR9QN8-P
  skos:prefLabel "drug therapy (Qualifier)"@en, "traitement médicamenteux (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-VQ7DWFHZ-Z
  skos:prefLabel "Adrenoleukodystrophy"@en, "Adrénoleucodystrophie"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

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

jvr:-CB30NGKB-3
  skos:prefLabel "economics (Qualifier)"@en, "économie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-D7ZX09M4-S
  skos:prefLabel "Peroxisomes"@en, "Péroxysomes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-MQ2BL28X-C .

jvr:-HM541ZMH-6
  skos:prefLabel "Zellweger Syndrome"@en, "Syndrome de Zellweger"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr:-CSKTXWF5-F
  skos:prefLabel "epidemiology (Qualifier)"@en, "épidémiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-BT300B3G-Q
  skos:prefLabel "cerebrospinal fluid (Qualifier)"@en, "liquide cérébrospinal (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-JVKFK2NX-2
  skos:prefLabel "nursing (Qualifier)"@en, "soins infirmiers (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-W4X1LN61-R
  skos:prefLabel "diet therapy (Qualifier)"@en, "diétothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-SS1XPWM3-C
  skos:prefLabel "Déficit en mévalonate kinase"@fr, "Mevalonate Kinase Deficiency"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-MQ2BL28X-C .

jvr:-RC3PND0F-S
  skos:prefLabel "ethnology (Qualifier)"@en, "ethnologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-XV06LPML-W
  skos:prefLabel "urine (Qualifier)"@en, "urine (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-NHL3D2X0-S
  skos:prefLabel "sang (Qualificatif)"@fr, "blood (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SBNWSM1T-R
  skos:prefLabel "history (Qualifier)"@en, "histoire (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .