> top > docs > PubMed:18412970 > spans > 0-284 > annotations

PubMed:18412970 / 0-284 JSONTXT

Annnotations TAB JSON ListView MergeView

c_corpus

Id Subject Object Predicate Lexical cue
T1 33-43 P42858 denotes huntingtin
T2 33-43 P42859 denotes huntingtin
T3 33-43 P51111 denotes huntingtin
T4 33-43 PR:000008840 denotes huntingtin
T5 33-43 P51112 denotes huntingtin
T6 85-95 P42858 denotes huntingtin
T7 85-95 P42859 denotes huntingtin
T8 85-95 P51111 denotes huntingtin
T9 85-95 PR:000008840 denotes huntingtin
T10 85-95 P51112 denotes huntingtin
T11 101-106 10090 denotes mouse
T12 101-106 D051379 denotes mouse
T13 107-116 P02301 denotes embryonic
T14 107-116 PR:000029532 denotes embryonic
T15 146-159 C097188 denotes polyglutamine
T16 146-159 C097188 denotes polyglutamine
T17 173-183 P42858 denotes huntingtin
T18 173-183 P42859 denotes huntingtin
T19 173-183 P51111 denotes huntingtin
T20 173-183 PR:000008840 denotes huntingtin
T21 173-183 P51112 denotes huntingtin
T22 185-188 PR:P51111 denotes Htt
T23 185-188 PR:000015189 denotes Htt
T24 185-188 PR:Q76P24 denotes Htt
T25 185-188 PR:P31645 denotes Htt
T26 185-188 PR:P42859 denotes Htt
T27 185-188 PR:Q60857 denotes Htt
T28 185-188 PR:P42858 denotes Htt
T29 185-188 PR:000008840 denotes Htt
T34 190-197 SO:0000104 denotes protein
T31 190-197 CHEBI:36080 denotes protein
T32 190-197 CHEBI:11122 denotes protein
T33 190-197 PR:000000001 denotes protein
T30 190-197 GO:0003675 denotes protein
T39 212-232 D006816 denotes Huntington's disease
T40 212-232 D006816 denotes Huntington's disease
T43 239-242 PR:P51111 denotes Htt
T44 239-242 PR:000015189 denotes Htt
T45 239-242 PR:Q76P24 denotes Htt
T46 239-242 PR:P31645 denotes Htt
T47 239-242 PR:P42859 denotes Htt
T48 239-242 PR:Q60857 denotes Htt
T49 239-242 PR:P42858 denotes Htt
T50 239-242 PR:000008840 denotes Htt
T51 259-263 SO:0000704 denotes gene
T52 267-275 SO:0000159 denotes deletion

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 212-232 DiseaseOrPhenotypicFeature denotes Huntington's disease 0007739
T2 234-236 DiseaseOrPhenotypicFeature denotes HD 0007739

UseCases_ArguminSci_Discourse

Id Subject Object Predicate Lexical cue
T1 0-129 DRI_Background denotes Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null mouse embryonic fibroblasts.
T2 142-238 DRI_Challenge denotes The polyglutamine expansion in huntingtin (Htt) protein is a cause of Huntington's disease (HD).