PubMed:18681856 / 0-144
Annnotations
LitCoin-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-144 | Sentence | denotes | Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene. |
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
5436 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | MESH:C563786 |
5437 | 102-109 | SequenceVariant | denotes | p.M453T | DBSNP:rs121908864 |
5438 | 118-138 | GeneOrGeneProduct | denotes | thyrotropin receptor | NCBIGene:7253 |
LitCoin_Mondo
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 46-61 | DiseaseOrPhenotypicFeature | denotes | hyperthyroidism | 0004425 |
LitCoin-SeqVar
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 102-109 | SequenceVariant | denotes | p.M453T |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 118-138 | GeneOrGeneProduct | denotes | thyrotropin receptor |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-9 | GeneOrGeneProduct | denotes | Expanding |
T2 | 72-82 | GeneOrGeneProduct | denotes | activating |
T3 | 92-100 | GeneOrGeneProduct | denotes | mutation |
T4 | 118-138 | GeneOrGeneProduct | denotes | thyrotropin receptor |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T1 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | C563786 |
LitCoin-GeneOrGeneProduct-v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 118-138 | GeneOrGeneProduct | denotes | thyrotropin receptor |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | 0012203 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T1 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | C563786 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T1 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | C563786 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T74312 | 118-138 | GeneOrGeneProduct | denotes | thyrotropin receptor | |
T2566 | 31-61 | DiseaseOrPhenotypicFeature | denotes | non-autoimmune hyperthyroidism | C563786 |
T50756 | 102-109 | SequenceVariant | denotes | p.M453T |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-144 | Sentence | denotes | Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene. |
T1 | 0-144 | Sentence | denotes | Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene. |
PubCasesHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TI1 | 46-61 | HP:0000836 | denotes | hyperthyroidism |
tmVarCorpus
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 102-109 | ProteinMutation:p|SUB|M|453|T | denotes | p.M453T |