PubMed:17549393 / 0-85
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 4119 | 8-12 | GeneOrGeneProduct | denotes | IRF6 | NCBIGene:3664 |
| 4120 | 32-36 | SequenceVariant | denotes | Y67X | p|SUB|Y|67|X |
| 4121 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | MESH:C536528 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-85 | Sentence | denotes | A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome. |
LitCoin_Mondo
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | 0019508 |
LitCoin-SeqVar
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 32-36 | SequenceVariant | denotes | Y67X |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 2-7 | GeneOrGeneProduct | denotes | novel |
| T2 | 8-12 | GeneOrGeneProduct | denotes | IRF6 |
| T3 | 22-30 | GeneOrGeneProduct | denotes | mutation |
| T4 | 38-42 | GeneOrGeneProduct | denotes | in a |
| T5 | 76-84 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 2-7 | GeneOrGeneProduct | denotes | novel |
| T2 | 8-12 | GeneOrGeneProduct | denotes | IRF6 |
| T3 | 76-84 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T1 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | C536528 |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 8-12 | GeneOrGeneProduct | denotes | IRF6 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | 0019508 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | C536528 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T1 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | C536528 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T92598 | 8-12 | GeneOrGeneProduct | denotes | IRF6 | |
| T89410 | 62-84 | DiseaseOrPhenotypicFeature | denotes | Van der Woude syndrome | C536528 |
| T61975 | 32-36 | SequenceVariant | denotes | Y67X |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 8-12 | gene:3664 | denotes | IRF6 |
| T1 | 62-84 | disease:C0175697 | denotes | Van der Woude syndrome |
| R1 | T0 | T1 | associated_with | IRF6,Van der Woude syndrome |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 17549393-0#8#12#gene3664 | 8-12 | gene3664 | denotes | IRF6 |
| 17549393-0#62#84#diseaseC0175697 | 62-84 | diseaseC0175697 | denotes | Van der Woude syndrome |
| 8#12#gene366462#84#diseaseC0175697 | 17549393-0#8#12#gene3664 | 17549393-0#62#84#diseaseC0175697 | associated_with | IRF6,Van der Woude syndrome |
tmVarCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 32-36 | ProteinMutation:p|SUB|Y|67|X | denotes | Y67X |