PubMed:21684788 / 61-326 JSONTXT

{"project":"LitCoin-sentences","denotations":[{"id":"T2","span":{"begin":0,"end":265},"obj":"Sentence"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

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{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T3","span":{"begin":16,"end":24},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":83,"end":93},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":147,"end":154},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":164,"end":192},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":197,"end":203},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":260,"end":264},"obj":"GeneOrGeneProduct"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

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{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":147,"end":154},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":164,"end":192},"obj":"GeneOrGeneProduct"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T2","span":{"begin":0,"end":24},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":26,"end":29},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":83,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":95,"end":113},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0010031"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0700001"},{"id":"A4","pred":"mondo_id","subj":"T3","obj":"0010031"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0019269"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0001071"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T2","span":{"begin":0,"end":24},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":26,"end":29},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":37,"end":65},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":83,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":95,"end":113},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"ID:","subj":"T2","obj":"D016111"},{"id":"A3","pred":"ID:","subj":"T3","obj":"D016111"},{"id":"A4","pred":"ID:","subj":"T4","obj":"DISEASE"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D007057"},{"id":"A6","pred":"ID:","subj":"T6","obj":"D008607"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":26,"end":29},"obj":"ChemicalEntity"},{"id":"T3","span":{"begin":164,"end":192},"obj":"ChemicalEntity"},{"id":"T4","span":{"begin":236,"end":250},"obj":"ChemicalEntity"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"http://purl.obolibrary.org/obo/CHEBI_8984"},{"id":"A2","pred":"ID:","subj":"T1","obj":"http://purl.obolibrary.org/obo/CHEBI_144475"},{"id":"A3","pred":"ID:","subj":"T3","obj":"C038828"},{"id":"A4","pred":"ID:","subj":"T4","obj":"C001634"},{"id":"A5","pred":"ID:","subj":"T4","obj":"http://purl.obolibrary.org/obo/CHEBI_35746"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T2","span":{"begin":0,"end":24},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":26,"end":29},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":37,"end":65},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":83,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":95,"end":113},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"D016111"},{"id":"A3","pred":"#label","subj":"T3","obj":"D016111"},{"id":"A4","pred":"#label","subj":"T4","obj":"DISEASE"},{"id":"A5","pred":"#label","subj":"T5","obj":"D007057"},{"id":"A6","pred":"#label","subj":"T6","obj":"D008607"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T4","span":{"begin":236,"end":250},"obj":"ChemicalEntity"},{"id":"T3","span":{"begin":164,"end":192},"obj":"ChemicalEntity"},{"id":"T1","span":{"begin":26,"end":29},"obj":"ChemicalEntity"},{"id":"T2","span":{"begin":164,"end":192},"obj":"GeneOrGeneProduct"},{"id":"T53498","span":{"begin":147,"end":154},"obj":"GeneOrGeneProduct"},{"id":"T85215","span":{"begin":95,"end":113},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T85524","span":{"begin":83,"end":93},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T36180","span":{"begin":37,"end":65},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T31910","span":{"begin":26,"end":29},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T37692","span":{"begin":0,"end":24},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A5","pred":"ID:","subj":"T4","obj":"http://purl.obolibrary.org/obo/CHEBI_35746"},{"id":"A4","pred":"ID:","subj":"T4","obj":"C001634"},{"id":"A3","pred":"ID:","subj":"T3","obj":"C038828"},{"id":"A2","pred":"ID:","subj":"T1","obj":"http://purl.obolibrary.org/obo/CHEBI_144475"},{"id":"A1","pred":"ID:","subj":"T1","obj":"http://purl.obolibrary.org/obo/CHEBI_8984"},{"id":"A14125","pred":"#label","subj":"T85215","obj":"D008607"},{"id":"A66494","pred":"#label","subj":"T85524","obj":"D007057"},{"id":"A41640","pred":"#label","subj":"T36180","obj":"DISEASE"},{"id":"A96244","pred":"#label","subj":"T31910","obj":"D016111"},{"id":"A76808","pred":"#label","subj":"T37692","obj":"D016111"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":164,"end":192},"obj":"gene:224"},{"id":"T1","span":{"begin":0,"end":24},"obj":"disease:C0037231"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":37,"end":56},"obj":"HP_0000007"},{"id":"T2","span":{"begin":83,"end":93},"obj":"HP_0008064"},{"id":"T3","span":{"begin":95,"end":113},"obj":"HP_0001249"},{"id":"T4","span":{"begin":115,"end":125},"obj":"HP_0001257"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"Allie","denotations":[{"id":"SS2_21684788_1_0","span":{"begin":26,"end":29},"obj":"abbr"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}

{"project":"PubCasesHPO","denotations":[{"id":"AB1","span":{"begin":83,"end":93},"obj":"HP:0008064"},{"id":"AB2","span":{"begin":115,"end":125},"obj":"HP:0001257"}],"text":"Sjögren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, spasticity and mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase, an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid."}