> top > projects > c_corpus > docs > PubMed:21540131 > annotations
c_corpus  

PubMed:21540131 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 39-42 PR:P51111 denotes HTT
T2 39-42 PR:000015189 denotes HTT
T3 39-42 PR:Q76P24 denotes HTT
T4 39-42 PR:P31645 denotes HTT
T5 39-42 PR:P42859 denotes HTT
T6 39-42 PR:Q60857 denotes HTT
T7 39-42 PR:P42858 denotes HTT
T8 39-42 PR:000008840 denotes HTT
T9 43-46 CVCL_D569 denotes CAG
T10 47-53 SO:0001068 denotes repeat
T15 69-89 D006816 denotes Huntington's disease
T16 69-89 D006816 denotes Huntington's disease
T23 103-123 D006816 denotes Huntington's disease
T24 103-123 D006816 denotes Huntington's disease
T27 146-164 C566739 denotes autosomal dominant
T30 165-191 D019636 denotes neurodegenerative disorder
T31 165-191 D019636 denotes neurodegenerative disorder
T32 204-207 CVCL_D569 denotes CAG
T33 208-214 SO:0001068 denotes repeat
T34 235-239 SO:0000704 denotes gene
T35 241-244 PR:P51111 denotes HTT
T36 241-244 PR:000015189 denotes HTT
T37 241-244 PR:Q76P24 denotes HTT
T38 241-244 PR:P31645 denotes HTT
T39 241-244 PR:P42859 denotes HTT
T40 241-244 PR:Q60857 denotes HTT
T41 241-244 PR:P42858 denotes HTT
T42 241-244 PR:000008840 denotes HTT
T43 251-254 CVCL_D569 denotes CAG
T44 255-261 SO:0000417 denotes domain
T45 272-275 PR:P51111 denotes HTT
T46 272-275 PR:000015189 denotes HTT
T47 272-275 PR:Q76P24 denotes HTT
T48 272-275 PR:P31645 denotes HTT
T49 272-275 PR:P42859 denotes HTT
T50 272-275 PR:Q60857 denotes HTT
T51 272-275 PR:P42858 denotes HTT
T52 272-275 PR:000008840 denotes HTT
T53 453-456 GO:0005574 denotes DNA
T55 453-456 SO:0000352 denotes DNA
T54 453-456 CHEBI:16991 denotes DNA
T56 453-456 D004247 denotes DNA
T57 510-513 CVCL_D569 denotes CAG
T58 581-584 CVCL_D569 denotes CAG
T59 585-591 SO:0001068 denotes repeat
T60 626-629 PR:P51111 denotes HTT
T61 626-629 PR:000015189 denotes HTT
T62 626-629 PR:Q76P24 denotes HTT
T63 626-629 PR:P31645 denotes HTT
T64 626-629 PR:P42859 denotes HTT
T65 626-629 PR:Q60857 denotes HTT
T66 626-629 PR:P42858 denotes HTT
T67 626-629 PR:000008840 denotes HTT
T68 808-811 CVCL_D569 denotes CAG
T69 812-818 SO:0001068 denotes repeat
T70 908-911 CVCL_D569 denotes CAG
T71 912-918 SO:0001068 denotes repeat
T72 1005-1008 CVCL_D569 denotes CAG
T73 1009-1015 SO:0001068 denotes repeat
T74 1077-1080 CVCL_D569 denotes CAG
T75 1081-1087 SO:0001068 denotes repeat
T76 1186-1189 CVCL_D569 denotes CAG
T77 1190-1196 SO:0001068 denotes repeat
T78 1242-1245 CVCL_D569 denotes CAG
T79 1246-1252 SO:0001068 denotes repeat
T80 1332-1335 CVCL_D569 denotes CAG
T81 1336-1342 SO:0001068 denotes repeat
T82 1362-1368 SO:0001023 denotes allele
T83 1409-1412 CVCL_D569 denotes CAG
T84 1413-1419 SO:0001068 denotes repeat
T85 1528-1531 CVCL_D569 denotes CAG
T86 1532-1538 SO:0001068 denotes repeat
T88 1674-1677 PR:P51111 denotes HTT
T89 1674-1677 PR:000015189 denotes HTT
T90 1674-1677 PR:Q76P24 denotes HTT
T91 1674-1677 PR:P31645 denotes HTT
T92 1674-1677 PR:P42859 denotes HTT
T93 1674-1677 PR:Q60857 denotes HTT
T94 1674-1677 PR:P42858 denotes HTT
T95 1674-1677 PR:000008840 denotes HTT
T96 1678-1681 CVCL_D569 denotes CAG
T97 1682-1688 SO:0001068 denotes repeat
T98 1786-1789 PR:P51111 denotes HTT
T99 1786-1789 PR:000015189 denotes HTT
T100 1786-1789 PR:Q76P24 denotes HTT
T101 1786-1789 PR:P31645 denotes HTT
T102 1786-1789 PR:P42859 denotes HTT
T103 1786-1789 PR:Q60857 denotes HTT
T104 1786-1789 PR:P42858 denotes HTT
T105 1786-1789 PR:000008840 denotes HTT
T106 1790-1793 CVCL_D569 denotes CAG
T107 1794-1800 SO:0001068 denotes repeat