PubMed:20143913 / 0-308 JSONTXT

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{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":39,"end":54},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":205,"end":220},"obj":"ChemicalEntity"},{"id":"T3","span":{"begin":222,"end":226},"obj":"ChemicalEntity"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D020051"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D020051"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D020051"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient.\nApparent homozygosity for the mutation p.R315X present on exon 5 of the arylsulfatase B (ARSB) gene in a mucopolysaccharidosis type VI patient was solved in this study by furt"}

{"project":"LitCoin-training-merged","denotations":[{"id":"T3","span":{"begin":222,"end":226},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":205,"end":220},"obj":"ChemicalEntity"},{"id":"T1","span":{"begin":39,"end":54},"obj":"ChemicalEntity"},{"id":"T46094","span":{"begin":222,"end":226},"obj":"GeneOrGeneProduct"},{"id":"T22214","span":{"begin":205,"end":220},"obj":"GeneOrGeneProduct"},{"id":"T37591","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"},{"id":"T95114","span":{"begin":238,"end":267},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T98066","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T11111","span":{"begin":268,"end":275},"obj":"OrganismTaxon"},{"id":"T14962","span":{"begin":124,"end":131},"obj":"OrganismTaxon"},{"id":"T47921","span":{"begin":172,"end":179},"obj":"SequenceVariant"}],"attributes":[{"id":"A3","pred":"ID:","subj":"T3","obj":"D020051"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D020051"},{"id":"A1","pred":"ID:","subj":"T1","obj":"D020051"},{"id":"A77747","pred":"#label","subj":"T95114","obj":"D009087"},{"id":"A5976","pred":"#label","subj":"T98066","obj":"D009087"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient.\nApparent homozygosity for the mutation p.R315X present on exon 5 of the arylsulfatase B (ARSB) gene in a mucopolysaccharidosis type VI patient was solved in this study by furt"}

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{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":238,"end":259},"obj":"HP_0008155"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient.\nApparent homozygosity for the mutation p.R315X present on exon 5 of the arylsulfatase B (ARSB) gene in a mucopolysaccharidosis type VI patient was solved in this study by furt"}

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{"project":"tmVarCorpus","denotations":[{"id":"T1","span":{"begin":172,"end":179},"obj":"ProteinMutation:p|SUB|R|315|X"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient.\nApparent homozygosity for the mutation p.R315X present on exon 5 of the arylsulfatase B (ARSB) gene in a mucopolysaccharidosis type VI patient was solved in this study by furt"}