PMC:1186732 / 3579-3744
Annnotations
craft-sa-dev
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T804 | 0-165 | sentence | denotes | Recent human genetic studies have also demonstrated mutations in this gene in Goldmann-Favre syndrome and many cases of clumped pigmentary retinal degeneration [5]. |
| T805 | 1-7 | JJ | denotes | Recent |
| T806 | 22-29 | NNS | denotes | studies |
| T807 | 8-13 | JJ | denotes | human |
| T808 | 14-21 | JJ | denotes | genetic |
| T809 | 40-52 | VBN | denotes | demonstrated |
| T810 | 30-34 | VBP | denotes | have |
| T811 | 35-39 | RB | denotes | also |
| T812 | 53-62 | NNS | denotes | mutations |
| T813 | 63-65 | IN | denotes | in |
| T814 | 66-70 | DT | denotes | this |
| T815 | 71-75 | NN | denotes | gene |
| T816 | 76-78 | IN | denotes | in |
| T817 | 79-87 | NNP | denotes | Goldmann |
| T818 | 88-93 | NNP | denotes | Favre |
| T819 | 87-88 | HYPH | denotes | - |
| T820 | 94-102 | NN | denotes | syndrome |
| T821 | 103-106 | CC | denotes | and |
| T822 | 107-111 | JJ | denotes | many |
| T823 | 112-117 | NNS | denotes | cases |
| T824 | 118-120 | IN | denotes | of |
| T825 | 121-128 | VBN | denotes | clumped |
| T826 | 148-160 | NN | denotes | degeneration |
| T827 | 129-139 | JJ | denotes | pigmentary |
| T828 | 140-147 | JJ | denotes | retinal |
| T829 | 161-162 | -LRB- | denotes | [ |
| T830 | 162-163 | CD | denotes | 5 |
| T831 | 163-164 | -RRB- | denotes | ] |
| T832 | 164-165 | . | denotes | . |
| R391 | T805 | T806 | amod | Recent,studies |
| R392 | T806 | T809 | nsubj | studies,demonstrated |
| R393 | T807 | T806 | amod | human,studies |
| R394 | T808 | T806 | amod | genetic,studies |
| R395 | T810 | T809 | aux | have,demonstrated |
| R396 | T811 | T809 | advmod | also,demonstrated |
| R397 | T812 | T809 | dobj | mutations,demonstrated |
| R398 | T813 | T809 | prep | in,demonstrated |
| R399 | T814 | T815 | det | this,gene |
| R400 | T815 | T813 | pobj | gene,in |
| R401 | T816 | T809 | prep | in,demonstrated |
| R402 | T817 | T818 | compound | Goldmann,Favre |
| R403 | T818 | T820 | compound | Favre,syndrome |
| R404 | T819 | T818 | punct | -,Favre |
| R405 | T820 | T816 | pobj | syndrome,in |
| R406 | T821 | T820 | cc | and,syndrome |
| R407 | T822 | T823 | amod | many,cases |
| R408 | T823 | T820 | conj | cases,syndrome |
| R409 | T824 | T823 | prep | of,cases |
| R410 | T825 | T826 | amod | clumped,degeneration |
| R411 | T826 | T824 | pobj | degeneration,of |
| R412 | T827 | T826 | amod | pigmentary,degeneration |
| R413 | T828 | T826 | amod | retinal,degeneration |
| R414 | T829 | T830 | punct | [,5 |
| R415 | T830 | T809 | parataxis | 5,demonstrated |
| R416 | T831 | T830 | punct | ],5 |
| R417 | T832 | T809 | punct | .,demonstrated |
craft-ca-core-ex-dev
Below, discontinuous spans are shown in the chain model. You can change it to the bag model.
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T637 | 8-13 | NCBITaxon:9606 | denotes | human |
| T638 | 14-21 | SO_EXT:0000704 | denotes | genetic |
| T639 | 53-62 | SO_EXT:sequence_alteration_entity_or_process | denotes | mutations |
| T640 | 71-75 | SO_EXT:0000704 | denotes | gene |
| T641 | 129-139 | CHEBI_EXT:26130 | denotes | pigmentary |
| T642 | 140-147 | UBERON:0000966 | denotes | retinal |
craft-ca-core-dev
Below, discontinuous spans are shown in the chain model. You can change it to the bag model.
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T569 | 8-13 | NCBITaxon:9606 | denotes | human |
| T570 | 14-21 | SO:0000704 | denotes | genetic |
| T571 | 71-75 | SO:0000704 | denotes | gene |
| T572 | 129-139 | CHEBI:26130 | denotes | pigmentary |
| T573 | 140-147 | UBERON:0000966 | denotes | retinal |
2_test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 16110338-12963616-85798502 | 162-163 | 12963616 | denotes | 5 |
| T58203 | 162-163 | 12963616 | denotes | 5 |