PubMed:25054547 / 0-88 JSONTXT

{"project":"LitCoin-entities","denotations":[{"id":"10153","span":{"begin":28,"end":32},"obj":"GeneOrGeneProduct"},{"id":"10154","span":{"begin":66,"end":77},"obj":"SequenceVariant"}],"attributes":[{"id":"A1","pred":"db_id","subj":"10153","obj":"NCBIGene:590"},{"id":"A2","pred":"db_id","subj":"10154","obj":"p|SUB|V|204|D"}],"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":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}

{"project":"LitCoin-SeqVar","denotations":[{"id":"T1","span":{"begin":66,"end":77},"obj":"SequenceVariant"}],"text":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":22,"end":27},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":28,"end":32},"obj":"GeneOrGeneProduct"}],"text":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":22,"end":27},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":28,"end":32},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":50,"end":55},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":56,"end":64},"obj":"GeneOrGeneProduct"}],"text":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":28,"end":32},"obj":"GeneOrGeneProduct"}],"text":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}

{"project":"LitCoin-training-merged","denotations":[{"id":"T44130","span":{"begin":28,"end":32},"obj":"GeneOrGeneProduct"},{"id":"T10402","span":{"begin":66,"end":77},"obj":"SequenceVariant"}],"text":"Characterization of a novel BCHE \"silent\" allele: point mutation (p.Val204Asp) causes lo"}