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PubMed:18470323 / 0-143 JSONTXT

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test-210614

Id Subject Object Predicate Lexical cue proteinmutation
18470323_0 63-68 ProteinMutation denotes R124C rs121909210

PubTator4TogoVar

Id Subject Object Predicate Lexical cue proteinmutation
18470323_0 63-68 ProteinMutation denotes R124C rs121909210

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-104 Sentence denotes Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.
T2 105-113 Sentence denotes PURPOSE:

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
5076 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I MESH:C537881
5077 63-68 SequenceVariant denotes R124C DBSNP:rs121909210
5078 85-90 GeneOrGeneProduct denotes TGFBI NCBIGene:7045
5079 92-97 GeneOrGeneProduct denotes BIGH3 NCBIGene:7045

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I 0007380
T2 25-50 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy 0004686
T3 33-50 DiseaseOrPhenotypicFeature denotes corneal dystrophy 0018102

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T1 63-68 SequenceVariant denotes R124C

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 51-57 GeneOrGeneProduct denotes type I
T2 85-90 GeneOrGeneProduct denotes TGFBI
T3 92-97 GeneOrGeneProduct denotes BIGH3

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 51-57 GeneOrGeneProduct denotes type I
T2 69-77 GeneOrGeneProduct denotes mutation
T3 85-90 GeneOrGeneProduct denotes TGFBI
T4 92-97 GeneOrGeneProduct denotes BIGH3

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 33-50 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T1 85-90 GeneOrGeneProduct denotes TGFBI
T2 92-97 GeneOrGeneProduct denotes BIGH3

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I 0007380

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I 0007380

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 33-50 DiseaseOrPhenotypicFeature denotes corneal dystrophy D003317

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I C537881

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T2 92-97 GeneOrGeneProduct denotes BIGH3
T55442 85-90 GeneOrGeneProduct denotes TGFBI
T50708 25-57 DiseaseOrPhenotypicFeature denotes lattice corneal dystrophy type I C537881
T23491 63-68 SequenceVariant denotes R124C

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-104 Sentence denotes Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.
TextSentencer_T2 105-113 Sentence denotes PURPOSE:
T1 0-104 Sentence denotes Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.
T2 105-113 Sentence denotes PURPOSE:

DisGeNET

Id Subject Object Predicate Lexical cue
T0 85-90 gene:7045 denotes TGFBI
T1 25-57 disease:C1690006 denotes lattice corneal dystrophy type I
T2 92-97 gene:7045 denotes BIGH3
T3 25-57 disease:C1690006 denotes lattice corneal dystrophy type I
R1 T0 T1 associated_with TGFBI,lattice corneal dystrophy type I
R2 T2 T3 associated_with BIGH3,lattice corneal dystrophy type I

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
18470323-0#63#68#geners121909210 63-68 geners121909210 denotes R124C
18470323-0#25#57#diseaseC1690006 25-57 diseaseC1690006 denotes lattice corneal dystrophy type I
63#68#geners12190921025#57#diseaseC1690006 18470323-0#63#68#geners121909210 18470323-0#25#57#diseaseC1690006 associated_with R124C,lattice corneal dystrophy type I

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
18470323-0#85#90#gene7045 85-90 gene7045 denotes TGFBI
18470323-0#92#97#gene7045 92-97 gene7045 denotes BIGH3
18470323-0#25#57#diseaseC1690006 25-57 diseaseC1690006 denotes lattice corneal dystrophy type I
85#90#gene704525#57#diseaseC1690006 18470323-0#85#90#gene7045 18470323-0#25#57#diseaseC1690006 associated_with TGFBI,lattice corneal dystrophy type I
92#97#gene704525#57#diseaseC1690006 18470323-0#92#97#gene7045 18470323-0#25#57#diseaseC1690006 associated_with BIGH3,lattice corneal dystrophy type I

PubCasesHPO

Id Subject Object Predicate Lexical cue
TI1 25-50 HP:0001149 denotes lattice corneal dystrophy

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 25-57 ORDO:98964 denotes lattice corneal dystrophy type I

tmVarCorpus

Id Subject Object Predicate Lexical cue
T1 63-68 ProteinMutation:p|SUB|R|124|C denotes R124C