
PubMed:21903317 / 0-108
Annnotations
LitCoin-sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-108 | Sentence | denotes | Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD. |
LitCoin-entities-OrganismTaxon-PD
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 77-83 | OrganismTaxon | denotes | anemia | NCBItxid:12939 |
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
8851 | 53-58 | GeneOrGeneProduct | denotes | renin | NCBIGene:5972 |
8852 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | MESH:D000740 |
8853 | 85-98 | DiseaseOrPhenotypicFeature | denotes | hyperuricemia | MESH:D033461 |
8854 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | MESH:D051436 |
LitCoin_Mondo
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | 0002280 |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 19-27 | GeneOrGeneProduct | denotes | mutation |
T2 | 35-49 | GeneOrGeneProduct | denotes | signal peptide |
T3 | 53-58 | GeneOrGeneProduct | denotes | renin |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 35-49 | GeneOrGeneProduct | denotes | signal peptide |
T2 | 53-58 | GeneOrGeneProduct | denotes | renin |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T1 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | D000740 |
T2 | 85-98 | DiseaseOrPhenotypicFeature | denotes | hyperuricemia | D033461 |
T3 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-GeneOrGeneProduct-v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 35-49 | GeneOrGeneProduct | denotes | signal peptide |
T2 | 53-58 | GeneOrGeneProduct | denotes | renin |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | 0002280 |
T2 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | 0005300 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T1 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | D000740 |
T2 | 85-98 | DiseaseOrPhenotypicFeature | denotes | hyperuricemia | D033461 |
T3 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T1 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | D000740 |
T2 | 85-98 | DiseaseOrPhenotypicFeature | denotes | hyperuricemia | D033461 |
T3 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 |
LitCoin-Chemical-MeSH-CHEBI
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T1 | 53-58 | ChemicalEntity | denotes | renin | D012083 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
---|---|---|---|---|---|---|
T1 | 53-58 | ChemicalEntity | denotes | renin | D012083 | |
T60777 | 53-58 | GeneOrGeneProduct | denotes | renin | ||
T16831 | 35-49 | GeneOrGeneProduct | denotes | signal peptide | ||
T55177 | 104-107 | DiseaseOrPhenotypicFeature | denotes | CKD | D051436 | |
T15051 | 85-98 | DiseaseOrPhenotypicFeature | denotes | hyperuricemia | D033461 | |
T87390 | 77-83 | DiseaseOrPhenotypicFeature | denotes | anemia | D000740 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-108 | Sentence | denotes | Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD. |
T1 | 0-108 | Sentence | denotes | Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD. |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
21903317-0#53#58#gene5972 | 53-58 | gene5972 | denotes | renin |
21903317-0#77#83#diseaseC0002871 | 77-83 | diseaseC0002871 | denotes | anemia |
21903317-0#104#107#diseaseC1561643 | 104-107 | diseaseC1561643 | denotes | CKD |
53#58#gene597277#83#diseaseC0002871 | 21903317-0#53#58#gene5972 | 21903317-0#77#83#diseaseC0002871 | associated_with | renin,anemia |
53#58#gene5972104#107#diseaseC1561643 | 21903317-0#53#58#gene5972 | 21903317-0#104#107#diseaseC1561643 | associated_with | renin,CKD |
PubCasesHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TI1 | 77-83 | HP:0001903 | denotes | anemia |
TI2 | 85-98 | HP:0002149 | denotes | hyperuricemia |