PubMed:28642124 / 130-215
Annnotations
c_corpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T16 | 0-20 | D006816 | denotes | Huntington's disease |
| T17 | 0-20 | D006816 | denotes | Huntington's disease |
| T20 | 36-39 | CVCL_D569 | denotes | CAG |
| T21 | 40-46 | SO:0001068 | denotes | repeat |
| T22 | 64-74 | P42858 | denotes | huntingtin |
| T23 | 64-74 | P42859 | denotes | huntingtin |
| T24 | 64-74 | P51111 | denotes | huntingtin |
| T25 | 64-74 | PR:000008840 | denotes | huntingtin |
| T26 | 64-74 | P51112 | denotes | huntingtin |
| T27 | 75-79 | SO:0000704 | denotes | gene |
| T28 | 81-84 | PR:P51111 | denotes | HTT |
| T29 | 81-84 | PR:000015189 | denotes | HTT |
| T30 | 81-84 | PR:Q76P24 | denotes | HTT |
| T31 | 81-84 | PR:P31645 | denotes | HTT |
| T32 | 81-84 | PR:P42859 | denotes | HTT |
| T33 | 81-84 | PR:Q60857 | denotes | HTT |
| T34 | 81-84 | PR:P42858 | denotes | HTT |
| T35 | 81-84 | PR:000008840 | denotes | HTT |
UseCases_ArguminSci_Discourse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-85 | DRI_Approach | denotes | Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. |