PMC:1892049 / 4626-4827
Annnotations
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 |
|---|---|---|---|---|
| T6048 | 16-23 | SO_EXT:0000704 | denotes | genetic |
| T6049 | 73-81 | SO:0001817 | denotes | in-frame |
| T6050 | 82-90 | SO_EXT:sequence_deletion_entity_or_process | denotes | deletion |
| T6051 | 94-99 | SO_EXT:0000147 | denotes | exons |
| T6052 | 117-121 | SO_EXT:0000704 | denotes | gene |
| T6053 | 122-127 | PR_EXT:000009158 | denotes | Itpr1 |
| T6054 | 129-134 | PR_EXT:000009158 | denotes | Itpr1 |
| T6055 | 145-153 | SO_EXT:sequence_coding_function | denotes | encoding |
| T6056 | 154-181 | CHEBI_EXT:1D_myo_inositol_1_4_5_trisphosphate | denotes | inositol 1,4,5-triphosphate |
| T6057 | 154-190 | GO_EXT:0005220 | denotes | inositol 1,4,5-triphosphate receptor |
| T6058 | 154-192 | PR_EXT:000009158 | denotes | inositol 1,4,5-triphosphate receptor 1 |
| T6059 | 194-199 | PR_EXT:000009158 | denotes | Itpr1 |
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 |
|---|---|---|---|---|
| T5824 | 16-23 | SO:0000704 | denotes | genetic |
| T5825 | 73-81 | SO:0001817 | denotes | in-frame |
| T5826 | 94-99 | SO:0000147 | denotes | exons |
| T5827 | 117-121 | SO:0000704 | denotes | gene |
| T5828 | 122-127 | PR:000009158 | denotes | Itpr1 |
| T5829 | 129-134 | PR:000009158 | denotes | Itpr1 |
| T5830 | 154-192 | PR:000009158 | denotes | inositol 1,4,5-triphosphate receptor 1 |
| T5831 | 194-199 | PR:000009158 | denotes | Itpr1 |
craft-sa-dev
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T6628 | 0-201 | sentence | denotes | The underlying genetic lesion causing the opt phenotype is a homozygous in-frame deletion of exons 43 and 44 of the gene Itpr1 (Itpr1opt /opt), encoding inositol 1,4,5-triphosphate receptor 1 (Itpr1). |
| T6629 | 1-4 | DT | denotes | The |
| T6630 | 24-30 | NN | denotes | lesion |
| T6631 | 5-15 | VBG | denotes | underlying |
| T6632 | 16-23 | JJ | denotes | genetic |
| T6633 | 57-59 | VBZ | denotes | is |
| T6634 | 31-38 | VBG | denotes | causing |
| T6635 | 39-42 | DT | denotes | the |
| T6636 | 47-56 | NN | denotes | phenotype |
| T6637 | 43-46 | NN | denotes | opt |
| T6638 | 60-61 | DT | denotes | a |
| T6639 | 82-90 | NN | denotes | deletion |
| T6640 | 62-72 | JJ | denotes | homozygous |
| T6641 | 73-75 | IN | denotes | in |
| T6642 | 76-81 | NN | denotes | frame |
| T6643 | 75-76 | HYPH | denotes | - |
| T6644 | 91-93 | IN | denotes | of |
| T6645 | 94-99 | NNS | denotes | exons |
| T6646 | 100-102 | CD | denotes | 43 |
| T6647 | 103-106 | CC | denotes | and |
| T6648 | 107-109 | CD | denotes | 44 |
| T6649 | 110-112 | IN | denotes | of |
| T6650 | 113-116 | DT | denotes | the |
| T6651 | 122-127 | NN | denotes | Itpr1 |
| T6652 | 117-121 | NN | denotes | gene |
| T6653 | 128-129 | -LRB- | denotes | ( |
| T6654 | 139-142 | NN | denotes | opt |
| T6655 | 129-137 | NN | denotes | Itpr1opt |
| T6656 | 138-139 | HYPH | denotes | / |
| T6657 | 142-143 | -RRB- | denotes | ) |
| T6658 | 143-145 | , | denotes | , |
| T6659 | 145-153 | VBG | denotes | encoding |
| T6660 | 154-162 | NN | denotes | inositol |
| T6661 | 182-190 | NN | denotes | receptor |
| T6662 | 163-164 | CD | denotes | 1 |
| T6663 | 167-168 | CD | denotes | 5 |
| T6664 | 164-165 | , | denotes | , |
| T6665 | 165-166 | CD | denotes | 4 |
| T6666 | 166-167 | , | denotes | , |
| T6667 | 169-181 | NN | denotes | triphosphate |
| T6668 | 168-169 | HYPH | denotes | - |
| T6669 | 191-192 | CD | denotes | 1 |
| T6670 | 193-194 | -LRB- | denotes | ( |
| T6671 | 194-199 | NN | denotes | Itpr1 |
| T6672 | 199-200 | -RRB- | denotes | ) |
| T6673 | 200-201 | . | denotes | . |
| R615 | T6629 | T6630 | det | The,lesion |
| R616 | T6630 | T6633 | nsubj | lesion,is |
| R617 | T6631 | T6630 | amod | underlying,lesion |
| R618 | T6632 | T6630 | amod | genetic,lesion |
| R620 | T6634 | T6630 | acl | causing,lesion |
| R622 | T6635 | T6636 | det | the,phenotype |
| R623 | T6636 | T6634 | dobj | phenotype,causing |
| R624 | T6637 | T6636 | compound | opt,phenotype |
| R626 | T6638 | T6639 | det | a,deletion |
| R627 | T6639 | T6633 | attr | deletion,is |
| R628 | T6640 | T6639 | amod | homozygous,deletion |
| R629 | T6641 | T6642 | nmod | in,frame |
| R631 | T6642 | T6639 | compound | frame,deletion |
| R632 | T6643 | T6642 | punct | -,frame |
| R634 | T6644 | T6639 | prep | of,deletion |
| R635 | T6645 | T6646 | nmod | exons,43 |
| R636 | T6646 | T6644 | pobj | 43,of |
| R638 | T6647 | T6646 | cc | and,43 |
| R639 | T6648 | T6646 | conj | 44,43 |
| R640 | T6649 | T6646 | prep | of,43 |
| R642 | T6650 | T6651 | det | the,Itpr1 |
| R643 | T6651 | T6649 | pobj | Itpr1,of |
| R644 | T6652 | T6651 | compound | gene,Itpr1 |
| R646 | T6653 | T6654 | punct | (,opt |
| R647 | T6654 | T6651 | parataxis | opt,Itpr1 |
| R648 | T6655 | T6654 | compound | Itpr1opt,opt |
| R650 | T6656 | T6654 | punct | /,opt |
| R651 | T6657 | T6654 | punct | ),opt |
| R652 | T6658 | T6646 | punct | ", ",43 |
| R653 | T6659 | T6646 | acl | encoding,43 |
| R655 | T6660 | T6661 | nmod | inositol,receptor |
| R656 | T6661 | T6659 | dobj | receptor,encoding |
| R657 | T6662 | T6663 | nummod | 1,5 |
| R658 | T6663 | T6667 | nummod | 5,triphosphate |
| R659 | T6664 | T6663 | punct | ",",5 |
| R660 | T6665 | T6663 | nummod | 4,5 |
| R661 | T6666 | T6663 | punct | ",",5 |
| R662 | T6667 | T6661 | compound | triphosphate,receptor |
| R663 | T6668 | T6667 | punct | -,triphosphate |
| R665 | T6669 | T6661 | nummod | 1,receptor |
| R666 | T6670 | T6671 | punct | (,Itpr1 |
| R667 | T6671 | T6661 | parataxis | Itpr1,receptor |
| R669 | T6672 | T6671 | punct | ),Itpr1 |
| R670 | T6673 | T6633 | punct | .,is |