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

vh8:-JBCF061Q-B
  skos:prefLabel "chromosome Y anormal"@fr, "abnormal Y chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-KKFB1G3D-6
  skos:prefLabel "chromosome sexuel anormal"@fr, "abnormal sex chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-ZSM8LBJ7-4
  skos:prefLabel "chromosome D anormal"@fr, "abnormal chromosome D"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-SNCJFLVZ-X
  skos:prefLabel "chromosome E16 anormal"@fr, "abnormal chromosome E16"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-L0ZDCF16-C
  skos:prefLabel "chromosome C anormal"@fr, "abnormal chromosome C"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-CZLZ683S-N
  skos:prefLabel "inversion péricentrique"@fr, "pericentric inversion"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-SCVWNBNB-D
  skos:prefLabel "translocation chromosomique"@fr, "chromosome translocation"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-BS4RQ2M0-W
  skos:prefLabel "chromosome C9 anormal"@fr, "abnormal chromosome C9"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-G65ZWL14-M
  skos:prefLabel "chromosome A1 anormal"@fr, "abnormal chromosome A1"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-ZXQNTJ7D-W
  skos:prefLabel "chromosome F anormal"@fr, "abnormal chromosome F"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-X94K6P1S-1
  skos:prefLabel "chromosome E18 anormal"@fr, "abnormal chromosome E18"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-DN2K8PWR-5
  skos:prefLabel "chromosome B4 anormal"@fr, "abnormal chromosome B4"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-TP0JR84G-G
  skos:prefLabel "microchromosome"@fr, "microcromosoma"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-SZRS9HH1-H
  skos:prefLabel "inversion chromosomique"@fr, "chromosome inversion"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-KBVM42F0-G
  skos:prefLabel "aberration chromosomique"@fr, "chromosomal aberration"@en ;
  a skos:Concept ;
  skos:narrower vh8:-R99WQ5B2-D .

vh8:-KXNFDBV3-1
  skos:prefLabel "isochromosome"@fr, "isocromosoma"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-SXD2SVZL-W
  skos:prefLabel "chromosome F20 anormal"@fr, "abnormal chromosome F20"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-L1FNNHF4-2
  skos:prefLabel "chromosome G21 anormal"@fr, "abnormal chromosome G21"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-NM2FS9LJ-4
  skos:prefLabel "chromosome X anormal"@fr, "abnormal X chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-ZN4930RT-F
  skos:prefLabel "chromosome E anormal"@fr, "abnormal chromosome E"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-N8F1FJGK-S
  skos:prefLabel "trisomie partielle"@fr, "partial trisomy"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-GSXMTL9V-6
  skos:prefLabel "chromosome F19 anormal"@fr, "abnormal chromosome F19"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-RXFLQKFF-W
  skos:prefLabel "chromosome E17 anormal"@fr, "abnormal chromosome E17"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-WKHFCMDL-H
  skos:prefLabel "chromosome double minute"@fr, "double minute chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-LR9LQV7M-0
  skos:prefLabel "duplication chromosomique"@fr, "chromosome duplication"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-D35D5RF7-1
  skos:prefLabel "chromosome D15 anormal"@fr, "abnormal chromosome D15"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-WPSLBHWV-0
  skos:prefLabel "chromosome annulaire"@fr, "ring chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-Q3F81H26-J
  skos:prefLabel "chromosome G anormal"@fr, "abnormal chromosome G"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-PB5PF0P5-2
  skos:prefLabel "chromosome B anormal"@fr, "abnormal chromosome B"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-DL9J32Z8-F
  skos:prefLabel "chromosome C12 anormal"@fr, "abnormal chromosome C12"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-RXG0ZKLW-N
  skos:prefLabel "chromosome A2 anormal"@fr, "abnormal chromosome A2"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-VLMGWRBW-G
  skos:prefLabel "inversion paracentrique"@fr, "paracentric inversion"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-TSXZX7B1-R
  skos:prefLabel "chromosome C11 anormal"@fr, "abnormal chromosome C11"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-H9F6VJ33-7
  skos:prefLabel "chromosome D13 anormal"@fr, "abnormal chromosome D13"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-PDS1RSSR-D
  skos:prefLabel "insertion chromosomique"@fr, "chromosome insertion"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-J19GBQCX-G
  skos:prefLabel "chromosome composé"@fr, "compound chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-F5C35H5P-V
  skos:prefLabel "chromosome D14 anormal"@fr, "abnormal chromosome D14"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-LJ2QJGJW-6
  skos:prefLabel "chromosome G22 anormal"@fr, "abnormal chromosome G22"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-KWSPWJ0L-2
  skos:prefLabel "chromosome C10 anormal"@fr, "abnormal chromosome C10"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-S9HDWXHT-R
  skos:prefLabel "deletion"@en, "délétion"@fr ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-GGBMZ6M0-D
  skos:prefLabel "autosome anormal"@fr, "abnormal autosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-GV97171K-C
  skos:prefLabel "fission centrique"@fr, "centric fission"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-T2G0TX1V-9
  skos:prefLabel "chromosome dicentrique"@fr, "dicentric chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-R99WQ5B2-D
  skos:narrower vh8:-KXNFDBV3-1, vh8:-SXD2SVZL-W, vh8:-RPL96KZ3-4, vh8:-B1DCD686-Q, vh8:-TP0JR84G-G, vh8:-D35D5RF7-1, vh8:-DCRMSX6Q-T, vh8:-N8F1FJGK-S, vh8:-CZLZ683S-N, vh8:-W6K39Z4G-C, vh8:-GV97171K-C, vh8:-HDRLLXHD-9, vh8:-RXG0ZKLW-N, vh8:-PB5PF0P5-2, vh8:-WKHFCMDL-H, vh8:-KKFB1G3D-6, vh8:-LJ2QJGJW-6, vh8:-GSXMTL9V-6, vh8:-H9F6VJ33-7, vh8:-ZXQNTJ7D-W, vh8:-X94K6P1S-1, vh8:-ZN4930RT-F, vh8:-B1TBFVM2-K, vh8:-SNCJFLVZ-X, vh8:-L0ZDCF16-C, vh8:-T2G0TX1V-9, vh8:-NM2FS9LJ-4, vh8:-PDS1RSSR-D, vh8:-Q3F81H26-J, vh8:-JBCF061Q-B, vh8:-SCVWNBNB-D, vh8:-F5C35H5P-V, vh8:-L1FNNHF4-2, vh8:-TSXZX7B1-R, vh8:-J19GBQCX-G, vh8:-WPSLBHWV-0, vh8:-BS4RQ2M0-W, vh8:-DL9J32Z8-F, vh8:-RXFLQKFF-W, vh8:-LR9LQV7M-0, vh8:-SZRS9HH1-H, vh8:-S9HDWXHT-R, vh8:-G65ZWL14-M, vh8:-GGBMZ6M0-D, vh8:-DN2K8PWR-5, vh8:-VLMGWRBW-G, vh8:-ZSM8LBJ7-4, vh8:-KWSPWJ0L-2, vh8:-MJ5F8VGV-N ;
  skos:broader vh8:-KBVM42F0-G ;
  skos:prefLabel "abnormal chromosome"@en, "chromosome anormal"@fr ;
  skos:inScheme vh8: ;
  a skos:Concept .

vh8:-HDRLLXHD-9
  skos:prefLabel "chromosome C7 anormal"@fr, "abnormal chromosome C7"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-B1TBFVM2-K
  skos:prefLabel "chromosome B5 anormal"@fr, "abnormal chromosome B5"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-DCRMSX6Q-T
  skos:prefLabel "chromosome A3 anormal"@fr, "abnormal chromosome A3"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-B1DCD686-Q
  skos:prefLabel "chromosome A anormal"@fr, "abnormal chromosome A"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8: a skos:ConceptScheme .
vh8:-RPL96KZ3-4
  skos:prefLabel "chromosome C6 anormal"@fr, "abnormal chromosome C6"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-MJ5F8VGV-N
  skos:prefLabel "chromosome Philadelphie"@fr, "Philadelphia chromosome"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .

vh8:-W6K39Z4G-C
  skos:prefLabel "chromosome C8 anormal"@fr, "abnormal chromosome C8"@en ;
  a skos:Concept ;
  skos:broader vh8:-R99WQ5B2-D .