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PubMed:21903317 / 0-108 JSONTXT

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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