PubMed:17059986 / 997-1199
Annnotations
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 0-202 | Sentence | denotes | Analysis of complementary DNA showed that the heterozygous nucleotide change c.2633+1G>C caused the appearance of 2 RNA molecules, 1 normal transcript and 1 skipping the entire exon 22 (r.2521_2634del). |
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 3551 | 77-88 | SequenceVariant | denotes | c.2633+1G>C | c|SUB|G|2633+1|C |
| 3552 | 186-200 | SequenceVariant | denotes | r.2521_2634del | r|DEL|2521_2634| |
LitCoin-SeqVar
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 77-88 | SequenceVariant | denotes | c.2633+1G>C |
| T4 | 186-200 | SequenceVariant | denotes | r.2521_2634del |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T15 | 140-150 | GeneOrGeneProduct | denotes | transcript |
| T16 | 151-156 | GeneOrGeneProduct | denotes | and 1 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T28 | 140-150 | GeneOrGeneProduct | denotes | transcript |
| T29 | 151-156 | GeneOrGeneProduct | denotes | and 1 |
| T30 | 157-165 | GeneOrGeneProduct | denotes | skipping |
| T31 | 170-176 | GeneOrGeneProduct | denotes | entire |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 140-156 | GeneOrGeneProduct | denotes | transcript and 1 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T69662 | 140-156 | GeneOrGeneProduct | denotes | transcript and 1 |
| T81029 | 186-200 | SequenceVariant | denotes | r.2521_2634del |
| T71586 | 77-88 | SequenceVariant | denotes | c.2633+1G>C |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T7 | 0-202 | Sentence | denotes | Analysis of complementary DNA showed that the heterozygous nucleotide change c.2633+1G>C caused the appearance of 2 RNA molecules, 1 normal transcript and 1 skipping the entire exon 22 (r.2521_2634del). |
| T7 | 0-202 | Sentence | denotes | Analysis of complementary DNA showed that the heterozygous nucleotide change c.2633+1G>C caused the appearance of 2 RNA molecules, 1 normal transcript and 1 skipping the entire exon 22 (r.2521_2634del). |
tmVarCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 77-88 | DNAMutation:c|SUB|G|2633+1|C | denotes | c.2633+1G>C |
| T4 | 186-200 | DNAMutation:r|DEL|2521_2634| | denotes | r.2521_2634del |