PubMed:15200408 / 1857-2135
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 923 | 125-134 | GeneOrGeneProduct | denotes | uroplakin | NCBIGene:11045|NCBIGene:7380 |
| 924 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | MESH:C564042 |
| 925 | 187-193 | OrganismTaxon | denotes | humans | NCBITaxon:9606 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T16 | 0-278 | Sentence | denotes | Such a weak association and the lack of families with simple dominant Mendelian inheritance suggest that missense changes of uroplakin genes cannot play a dominant role in causing VUR in humans, although they may be weak risk factors contributing to a complex polygenic disease. |
LitCoin-entities-OrganismTaxon-PD
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T5 | 187-193 | OrganismTaxon | denotes | humans | NCBItxid:9605 |
LitCoin_Mondo
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T5 | 80-91 | DiseaseOrPhenotypicFeature | denotes | inheritance | 0021152 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T42 | 7-11 | GeneOrGeneProduct | denotes | weak |
| T43 | 32-36 | GeneOrGeneProduct | denotes | lack |
| T44 | 54-60 | GeneOrGeneProduct | denotes | simple |
| T45 | 105-113 | GeneOrGeneProduct | denotes | missense |
| T46 | 180-183 | GeneOrGeneProduct | denotes | VUR |
| T47 | 216-220 | GeneOrGeneProduct | denotes | weak |
| T48 | 226-233 | GeneOrGeneProduct | denotes | factors |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T25 | 7-11 | GeneOrGeneProduct | denotes | weak |
| T26 | 32-36 | GeneOrGeneProduct | denotes | lack |
| T27 | 180-183 | GeneOrGeneProduct | denotes | VUR |
| T28 | 216-220 | GeneOrGeneProduct | denotes | weak |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T18 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | D014718 |
| T19 | 270-277 | DiseaseOrPhenotypicFeature | denotes | disease | D004194 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T27 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | 0008653|0006007 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T19 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | D014718 |
| T20 | 270-277 | DiseaseOrPhenotypicFeature | denotes | disease | D004194 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T18 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | D014718 |
LitCoin-NCBITaxon-2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T6 | 187-193 | OrganismTaxon | denotes | humans |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T18 | 180-183 | DiseaseOrPhenotypicFeature | denotes | VUR | D014718 |
| T60905 | 187-193 | OrganismTaxon | denotes | humans |