PubMed:19565319 / 468-769 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T5","span":{"begin":0,"end":301},"obj":"Sentence"}],"text":"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."}

{"project":"LitCoin-entities","denotations":[{"id":"6275","span":{"begin":3,"end":20},"obj":"DiseaseOrPhenotypicFeature"},{"id":"6276","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"},{"id":"6277","span":{"begin":92,"end":109},"obj":"DiseaseOrPhenotypicFeature"},{"id":"6278","span":{"begin":149,"end":152},"obj":"DiseaseOrPhenotypicFeature"},{"id":"6279","span":{"begin":201,"end":204},"obj":"DiseaseOrPhenotypicFeature"},{"id":"6280","span":{"begin":293,"end":300},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A14","pred":"db_id","subj":"6275","obj":"MESH:D001321"},{"id":"A15","pred":"db_id","subj":"6276","obj":"MESH:D004062"},{"id":"A16","pred":"db_id","subj":"6277","obj":"MESH:D004062"},{"id":"A17","pred":"db_id","subj":"6278","obj":"MESH:D000067877"},{"id":"A18","pred":"db_id","subj":"6279","obj":"MESH:D000067877"},{"id":"A19","pred":"db_id","subj":"6280","obj":"NCBIGene:135"}],"namespaces":[{"prefix":"_base","uri":"https://w3id.org/biolink/vocab/"},{"prefix":"MESH","uri":"http://id.nlm.nih.gov/mesh/"},{"prefix":"NCBITaxon","uri":"https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id="},{"prefix":"NCBIGene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"OMIM","uri":"https://www.omim.org/entry/"},{"prefix":"DBSNP","uri":"https://www.ncbi.nlm.nih.gov/snp/"}],"text":"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."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T7","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0018923"}],"text":"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."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T12","span":{"begin":72,"end":80},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":86,"end":91},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":114,"end":126},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":293,"end":300},"obj":"GeneOrGeneProduct"}],"text":"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."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T10","span":{"begin":72,"end":80},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":86,"end":91},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":293,"end":300},"obj":"GeneOrGeneProduct"}],"text":"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."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T7","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"originalLabel","subj":"T7","obj":"D004062"}],"text":"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."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T6","span":{"begin":293,"end":300},"obj":"GeneOrGeneProduct"}],"text":"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."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T13","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14","span":{"begin":149,"end":152},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T15","span":{"begin":201,"end":204},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"mondo_id","subj":"T13","obj":"0018923"},{"id":"A14","pred":"mondo_id","subj":"T14","obj":"0006664"},{"id":"A15","pred":"mondo_id","subj":"T15","obj":"0006664"}],"text":"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."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T9","span":{"begin":3,"end":20},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":92,"end":109},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":149,"end":152},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":201,"end":204},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"ID:","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"ID:","subj":"T10","obj":"D004062"},{"id":"A11","pred":"ID:","subj":"T11","obj":"DISEASE"},{"id":"A12","pred":"ID:","subj":"T12","obj":"DISEASE"},{"id":"A13","pred":"ID:","subj":"T13","obj":"DISEASE"}],"text":"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."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T9","span":{"begin":3,"end":20},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":92,"end":109},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":149,"end":152},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T13","span":{"begin":201,"end":204},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A9","pred":"#label","subj":"T9","obj":"DISEASE"},{"id":"A10","pred":"#label","subj":"T10","obj":"D004062"},{"id":"A11","pred":"#label","subj":"T11","obj":"DISEASE"},{"id":"A12","pred":"#label","subj":"T12","obj":"DISEASE"},{"id":"A13","pred":"#label","subj":"T13","obj":"DISEASE"}],"text":"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."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T6","span":{"begin":293,"end":300},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":201,"end":204},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T12","span":{"begin":149,"end":152},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11","span":{"begin":92,"end":109},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":55,"end":80},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":3,"end":20},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A13","pred":"#label","subj":"T13","obj":"DISEASE"},{"id":"A12","pred":"#label","subj":"T12","obj":"DISEASE"},{"id":"A11","pred":"#label","subj":"T11","obj":"DISEASE"},{"id":"A10","pred":"#label","subj":"T10","obj":"D004062"},{"id":"A9","pred":"#label","subj":"T9","obj":"DISEASE"}],"text":"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."}

{"project":"DisGeNET","denotations":[{"id":"T4","span":{"begin":201,"end":204},"obj":"gene:414"},{"id":"T5","span":{"begin":55,"end":80},"obj":"disease:C0012236"},{"id":"T6","span":{"begin":201,"end":204},"obj":"gene:414"},{"id":"T7","span":{"begin":55,"end":80},"obj":"disease:C0220704"}],"relations":[{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"},{"id":"R4","pred":"associated_with","subj":"T6","obj":"T7"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"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."}