PubMed:16120104 / 1522-1623
Annnotations
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T9 | 0-101 | Sentence | denotes | The PER2 111G allele associates with morning preference and is a potential candidate allele for ASPS. |
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 2223 | 4-8 | GeneOrGeneProduct | denotes | PER2 | NCBIGene:8864 |
| 2224 | 9-13 | SequenceVariant | denotes | 111G | c|Allele|G|111 |
| 2225 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | MESH:C565789 |
LitCoin-SeqVar
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 9-13 | SequenceVariant | denotes | 111G |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T37 | 4-8 | GeneOrGeneProduct | denotes | PER2 |
| T38 | 37-44 | GeneOrGeneProduct | denotes | morning |
| T39 | 96-100 | GeneOrGeneProduct | denotes | ASPS |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T20 | 4-8 | GeneOrGeneProduct | denotes | PER2 |
| T21 | 96-100 | GeneOrGeneProduct | denotes | ASPS |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T3 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | D020178 |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T8 | 4-8 | GeneOrGeneProduct | denotes | PER2 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T5 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | 0024378|0011655 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T3 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | D020178 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T3 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | D020178 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T8 | 4-8 | GeneOrGeneProduct | denotes | PER2 | |
| T78707 | 96-100 | DiseaseOrPhenotypicFeature | denotes | ASPS | D020178 |
| T70738 | 9-13 | SequenceVariant | denotes | 111G |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 16120104-8#4#8#gene8864 | 4-8 | gene8864 | denotes | PER2 |
| 16120104-8#96#100#diseaseC0206657 | 96-100 | diseaseC0206657 | denotes | ASPS |
| 4#8#gene886496#100#diseaseC0206657 | 16120104-8#4#8#gene8864 | 16120104-8#96#100#diseaseC0206657 | associated_with | PER2,ASPS |