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PubMed:21684788 / 0-174 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T1 0-60 Sentence denotes Large contiguous gene deletions in Sjögren-Larsson syndrome.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
8694 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome MESH:D016111
8695 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome MESH:D016111
8696 87-90 DiseaseOrPhenotypicFeature denotes SLS MESH:D016111
8697 98-126 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder MESH:D030342
8698 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis MESH:D007057
8699 156-174 DiseaseOrPhenotypicFeature denotes mental retardation MESH:D008607

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T1 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome 0010031
T2 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome 0010031
T3 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis 0019269

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T1 0-5 GeneOrGeneProduct denotes Large
T2 51-59 GeneOrGeneProduct denotes syndrome
T3 77-85 GeneOrGeneProduct denotes syndrome
T4 144-154 GeneOrGeneProduct denotes ichthyosis

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T1 0-5 GeneOrGeneProduct denotes Large
T2 51-59 GeneOrGeneProduct denotes syndrome
T3 77-85 GeneOrGeneProduct denotes syndrome
T4 144-154 GeneOrGeneProduct denotes ichthyosis

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T1 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T2 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T3 87-90 DiseaseOrPhenotypicFeature denotes SLS D016111
T4 98-126 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder DISEASE
T5 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis D007057
T6 156-174 DiseaseOrPhenotypicFeature denotes mental retardation D008607

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T1 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome 0010031
T2 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome 0010031
T3 87-90 DiseaseOrPhenotypicFeature denotes SLS 0700001|0010031
T5 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis 0019269
T6 156-174 DiseaseOrPhenotypicFeature denotes mental retardation 0001071

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T1 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T2 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T3 87-90 DiseaseOrPhenotypicFeature denotes SLS D016111
T4 98-126 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder DISEASE
T5 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis D007057
T6 156-174 DiseaseOrPhenotypicFeature denotes mental retardation D008607

LitCoin-Chemical-MeSH-CHEBI

Id Subject Object Predicate Lexical cue ID:
T1 87-90 ChemicalEntity denotes SLS http://purl.obolibrary.org/obo/CHEBI_8984|http://purl.obolibrary.org/obo/CHEBI_144475

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T1 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T2 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T3 87-90 DiseaseOrPhenotypicFeature denotes SLS D016111
T4 98-126 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder DISEASE
T5 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis D007057
T6 156-174 DiseaseOrPhenotypicFeature denotes mental retardation D008607

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label ID:
T1 87-90 ChemicalEntity denotes SLS http://purl.obolibrary.org/obo/CHEBI_144475|http://purl.obolibrary.org/obo/CHEBI_8984
T85215 156-174 DiseaseOrPhenotypicFeature denotes mental retardation D008607
T85524 144-154 DiseaseOrPhenotypicFeature denotes ichthyosis D007057
T36180 98-126 DiseaseOrPhenotypicFeature denotes autosomal recessive disorder DISEASE
T31910 87-90 DiseaseOrPhenotypicFeature denotes SLS D016111
T37692 61-85 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111
T18735 35-59 DiseaseOrPhenotypicFeature denotes Sjögren-Larsson syndrome D016111

DisGeNET

Id Subject Object Predicate Lexical cue
T1 61-85 disease:C0037231 denotes Sjögren-Larsson syndrome

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 98-117 HP_0000007 denotes autosomal recessive
T2 144-154 HP_0008064 denotes ichthyosis
T3 156-174 HP_0001249 denotes mental retardation

Allie

Id Subject Object Predicate Lexical cue
SS1_21684788_1_0 35-85 expanded denotes Sjögren-Larsson syndrome. Sjögren-Larsson syndrome
SS2_21684788_1_0 87-90 abbr denotes SLS
AE1_21684788_1_0 SS1_21684788_1_0 SS2_21684788_1_0 abbreviatedTo "Sjögren-Larsson syndrome. Sjögren-Larsson syndrome",SLS

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 144-154 HP:0008064 denotes ichthyosis