PubMed:18385794 / 0-168
Annnotations
PMID_GLOBAL
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | 0021129 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-129 | Sentence | denotes | Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. |
| T2 | 130-138 | Sentence | denotes | PURPOSE: |
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 4873 | 63-67 | GeneOrGeneProduct | denotes | SOX2 | NCBIGene:6657 |
| 4874 | 72-77 | GeneOrGeneProduct | denotes | CHX10 | NCBIGene:338917 |
| 4875 | 87-95 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
| 4876 | 101-113 | DiseaseOrPhenotypicFeature | denotes | anophthalmia | MESH:D000853 |
| 4877 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | MESH:D008850 |
| 4878 | 156-160 | GeneOrGeneProduct | denotes | SOX2 | NCBIGene:6657 |
LitCoin_Mondo
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | 0021129 |
LitCoin-NCBITaxon-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 87-95 | OrganismTaxon | denotes | patients |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 18-23 | GeneOrGeneProduct | denotes | novel |
| T2 | 63-67 | GeneOrGeneProduct | denotes | SOX2 |
| T3 | 72-77 | GeneOrGeneProduct | denotes | CHX10 |
| T4 | 114-128 | GeneOrGeneProduct | denotes | microphthalmia |
| T5 | 156-160 | GeneOrGeneProduct | denotes | SOX2 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 18-23 | GeneOrGeneProduct | denotes | novel |
| T2 | 24-33 | GeneOrGeneProduct | denotes | mutations |
| T3 | 63-67 | GeneOrGeneProduct | denotes | SOX2 |
| T4 | 72-77 | GeneOrGeneProduct | denotes | CHX10 |
| T5 | 114-128 | GeneOrGeneProduct | denotes | microphthalmia |
| T6 | 139-148 | GeneOrGeneProduct | denotes | Mutations |
| T7 | 156-160 | GeneOrGeneProduct | denotes | SOX2 |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T1 | 101-113 | DiseaseOrPhenotypicFeature | denotes | anophthalmia | D000853 |
| T2 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | D008850 |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 63-67 | GeneOrGeneProduct | denotes | SOX2 |
| T2 | 72-77 | GeneOrGeneProduct | denotes | CHX10 |
| T3 | 156-160 | GeneOrGeneProduct | denotes | SOX2 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | 0021129 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 101-113 | DiseaseOrPhenotypicFeature | denotes | anophthalmia | D000853 |
| T2 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | D008850 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T1 | 101-113 | DiseaseOrPhenotypicFeature | denotes | anophthalmia | D000853 |
| T2 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | D008850 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T3 | 156-160 | GeneOrGeneProduct | denotes | SOX2 | |
| T25444 | 72-77 | GeneOrGeneProduct | denotes | CHX10 | |
| T99114 | 63-67 | GeneOrGeneProduct | denotes | SOX2 | |
| T8193 | 114-128 | DiseaseOrPhenotypicFeature | denotes | microphthalmia | D008850 |
| T56294 | 101-113 | DiseaseOrPhenotypicFeature | denotes | anophthalmia | D000853 |
| T16555 | 87-95 | OrganismTaxon | denotes | patients |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 18385794-0#63#67#gene6657 | 63-67 | gene6657 | denotes | SOX2 |
| 18385794-0#101#113#diseaseC0003119 | 101-113 | diseaseC0003119 | denotes | anophthalmia |
| 63#67#gene6657101#113#diseaseC0003119 | 18385794-0#63#67#gene6657 | 18385794-0#101#113#diseaseC0003119 | associated_with | SOX2,anophthalmia |