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PubMed:19565319 / 468-769 JSONTXT

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LitCoin-sentences

Id Subject Object Predicate Lexical cue
T5 0-301 Sentence denotes As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
6275 3-20 DiseaseOrPhenotypicFeature denotes autistic symptoms MESH:D001321
6276 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome MESH:D004062
6277 92-109 DiseaseOrPhenotypicFeature denotes 22q11.2 deletions MESH:D004062
6278 149-152 DiseaseOrPhenotypicFeature denotes ASD MESH:D000067877
6279 201-204 DiseaseOrPhenotypicFeature denotes ASD MESH:D000067877
6280 293-300 GeneOrGeneProduct denotes ADORA2A NCBIGene:135

LitCoin_Mondo

Id Subject Object Predicate Lexical cue mondo_id
T7 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome 0018923

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T12 72-80 GeneOrGeneProduct denotes syndrome
T13 86-91 GeneOrGeneProduct denotes large
T14 114-126 GeneOrGeneProduct denotes duplications
T15 293-300 GeneOrGeneProduct denotes ADORA2A

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T10 72-80 GeneOrGeneProduct denotes syndrome
T11 86-91 GeneOrGeneProduct denotes large
T12 293-300 GeneOrGeneProduct denotes ADORA2A

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T7 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome D004062

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T6 293-300 GeneOrGeneProduct denotes ADORA2A

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T13 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome 0018923
T14 149-152 DiseaseOrPhenotypicFeature denotes ASD 0006664
T15 201-204 DiseaseOrPhenotypicFeature denotes ASD 0006664

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T9 3-20 DiseaseOrPhenotypicFeature denotes autistic symptoms DISEASE
T10 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome D004062
T11 92-109 DiseaseOrPhenotypicFeature denotes 22q11.2 deletions DISEASE
T12 149-152 DiseaseOrPhenotypicFeature denotes ASD DISEASE
T13 201-204 DiseaseOrPhenotypicFeature denotes ASD DISEASE

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T9 3-20 DiseaseOrPhenotypicFeature denotes autistic symptoms DISEASE
T10 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome D004062
T11 92-109 DiseaseOrPhenotypicFeature denotes 22q11.2 deletions DISEASE
T12 149-152 DiseaseOrPhenotypicFeature denotes ASD DISEASE
T13 201-204 DiseaseOrPhenotypicFeature denotes ASD DISEASE

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T6 293-300 GeneOrGeneProduct denotes ADORA2A
T13 201-204 DiseaseOrPhenotypicFeature denotes ASD DISEASE
T12 149-152 DiseaseOrPhenotypicFeature denotes ASD DISEASE
T11 92-109 DiseaseOrPhenotypicFeature denotes 22q11.2 deletions DISEASE
T10 55-80 DiseaseOrPhenotypicFeature denotes 22q11.2 deletion syndrome D004062
T9 3-20 DiseaseOrPhenotypicFeature denotes autistic symptoms DISEASE

DisGeNET

Id Subject Object Predicate Lexical cue
T4 201-204 gene:414 denotes ASD
T5 55-80 disease:C0012236 denotes 22q11.2 deletion syndrome
T6 201-204 gene:414 denotes ASD
T7 55-80 disease:C0220704 denotes 22q11.2 deletion syndrome
R3 T4 T5 associated_with ASD,22q11.2 deletion syndrome
R4 T6 T7 associated_with ASD,22q11.2 deletion syndrome