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PubMed:17033686 / 0-110 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
3446 32-37 GeneOrGeneProduct denotes PQBP1 NCBIGene:10084
3447 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia MESH:D008850
3448 78-90 DiseaseOrPhenotypicFeature denotes microcephaly MESH:D008831

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia 0021129
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 6-10 GeneOrGeneProduct denotes base
T2 11-15 GeneOrGeneProduct denotes pair
T3 32-37 GeneOrGeneProduct denotes PQBP1
T4 62-76 GeneOrGeneProduct denotes microphthalmia

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 32-37 GeneOrGeneProduct denotes PQBP1
T2 62-76 GeneOrGeneProduct denotes microphthalmia

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 32-37 GeneOrGeneProduct denotes PQBP1

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia 0021129
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly 0001149

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia D008850
T2 78-90 DiseaseOrPhenotypicFeature denotes microcephaly D008831

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T1 32-37 GeneOrGeneProduct denotes PQBP1
T61537 78-90 DiseaseOrPhenotypicFeature denotes microcephaly D008831
T21811 62-76 DiseaseOrPhenotypicFeature denotes microphthalmia D008850

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
17033686-0#32#37#gene10084 32-37 gene10084 denotes PQBP1
17033686-0#62#76#diseaseC0026010 62-76 diseaseC0026010 denotes microphthalmia
32#37#gene1008462#76#diseaseC0026010 17033686-0#32#37#gene10084 17033686-0#62#76#diseaseC0026010 associated_with PQBP1,microphthalmia

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 62-76 HP:0000568 denotes microphthalmia
TI2 78-90 HP:0000252 denotes microcephaly