PubMed:21903317 / 1093-1176
Annnotations
LitCoin-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T8 | 0-83 | Sentence | denotes | On this basis, we conclude that REN mutations are rare events in patients with CKD. |
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
8882 | 32-35 | GeneOrGeneProduct | denotes | REN | NCBIGene:5972 |
8883 | 65-73 | OrganismTaxon | denotes | patients | NCBITaxon:9606 |
8884 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | MESH:D051436 |
LitCoin_Mondo
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T7 | 50-54 | DiseaseOrPhenotypicFeature | denotes | rare | 0021136 |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T32 | 8-13 | GeneOrGeneProduct | denotes | basis |
T33 | 32-35 | GeneOrGeneProduct | denotes | REN |
T34 | 36-45 | GeneOrGeneProduct | denotes | mutations |
T35 | 50-54 | GeneOrGeneProduct | denotes | rare |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T22 | 32-35 | GeneOrGeneProduct | denotes | REN |
T23 | 50-54 | GeneOrGeneProduct | denotes | rare |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T13 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-GeneOrGeneProduct-v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T14 | 32-35 | GeneOrGeneProduct | denotes | REN |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T10 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | 0005300 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T15 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T14 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-NCBITaxon-2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 65-73 | OrganismTaxon | denotes | patients |
LitCoin-Chemical-MeSH-CHEBI
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T20 | 32-35 | ChemicalEntity | denotes | REN | D012083 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
---|---|---|---|---|---|---|
T20 | 32-35 | ChemicalEntity | denotes | REN | D012083 | |
T14 | 32-35 | GeneOrGeneProduct | denotes | REN | ||
T28823 | 79-82 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 | |
T28669 | 65-73 | OrganismTaxon | denotes | patients |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T8 | 0-83 | Sentence | denotes | On this basis, we conclude that REN mutations are rare events in patients with CKD. |
T8 | 0-83 | Sentence | denotes | On this basis, we conclude that REN mutations are rare events in patients with CKD. |