PubMed:15241482 / 229-373 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"966","span":{"begin":26,"end":31},"obj":"SequenceVariant"},{"id":"967","span":{"begin":36,"end":42},"obj":"SequenceVariant"},{"id":"968","span":{"begin":68,"end":75},"obj":"SequenceVariant"},{"id":"969","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A7","pred":"db_id","subj":"966","obj":"p|SUB|M|55|L"},{"id":"A8","pred":"db_id","subj":"967","obj":"p|SUB|Q|192|R"},{"id":"A9","pred":"db_id","subj":"968","obj":"c|SUB|C|-107|T"},{"id":"A10","pred":"db_id","subj":"969","obj":"MESH:D003327"}],"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":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-sentences","denotations":[{"id":"T3","span":{"begin":0,"end":144},"obj":"Sentence"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T1","span":{"begin":26,"end":29},"obj":"SequenceVariant"},{"id":"T2","span":{"begin":36,"end":40},"obj":"SequenceVariant"},{"id":"T3","span":{"begin":69,"end":73},"obj":"SequenceVariant"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T7","span":{"begin":86,"end":97},"obj":"GeneOrGeneProduct"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T4","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D003327"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T3","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0005010"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T4","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"ID:","subj":"T4","obj":"D003327"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T3","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"#label","subj":"T3","obj":"D003327"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T78486","span":{"begin":140,"end":143},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T36969","span":{"begin":69,"end":73},"obj":"SequenceVariant"},{"id":"T25380","span":{"begin":36,"end":40},"obj":"SequenceVariant"},{"id":"T73731","span":{"begin":26,"end":29},"obj":"SequenceVariant"}],"attributes":[{"id":"A70336","pred":"#label","subj":"T78486","obj":"D003327"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}

{"project":"DisGeNET5_variant_disease","denotations":[{"id":"15241482-2#26#31#geners854560","span":{"begin":26,"end":31},"obj":"geners854560"},{"id":"15241482-2#140#143#diseaseC0010068","span":{"begin":140,"end":143},"obj":"diseaseC0010068"}],"relations":[{"id":"26#31#geners854560140#143#diseaseC0010068","pred":"associated_with","subj":"15241482-2#26#31#geners854560","obj":"15241482-2#140#143#diseaseC0010068"}],"text":"Two coding polymorphisms, 55M/L and 192Q/R, and a promoter variant, -107C/T, has been extensively studied with respect to susceptibility to CHD."}