PubMed:20143913 / 0-132 JSONTXT

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    LitCoin-sentences

    {"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":132},"obj":"Sentence"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-entities

    {"project":"LitCoin-entities","denotations":[{"id":"7098","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"},{"id":"7099","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"},{"id":"7100","span":{"begin":124,"end":131},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"7098","obj":"NCBIGene:411"},{"id":"A2","pred":"db_id","subj":"7099","obj":"MESH:D009087"},{"id":"A3","pred":"db_id","subj":"7100","obj":"NCBITaxon:9606"}],"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":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin_Mondo

    {"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":94,"end":115},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0019249"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-GeneOrGeneProduct-v0

    {"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":0,"end":5},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":89,"end":93},"obj":"GeneOrGeneProduct"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-GeneOrGeneProduct-v2

    {"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":0,"end":5},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-Disease-MeSH

    {"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"D009087"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-GeneOrGeneProduct-v3

    {"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin_Mondo_095

    {"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0009661"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-MeSH-Disease-2

    {"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D009087"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-MONDO_bioort2019

    {"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D009087"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-NCBITaxon-2

    {"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":124,"end":131},"obj":"OrganismTaxon"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-Chemical-MeSH-CHEBI

    {"project":"LitCoin-Chemical-MeSH-CHEBI","denotations":[{"id":"T1","span":{"begin":39,"end":54},"obj":"ChemicalEntity"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D020051"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    LitCoin-training-merged

    {"project":"LitCoin-training-merged","denotations":[{"id":"T1","span":{"begin":39,"end":54},"obj":"ChemicalEntity"},{"id":"T37591","span":{"begin":39,"end":54},"obj":"GeneOrGeneProduct"},{"id":"T98066","span":{"begin":94,"end":123},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T14962","span":{"begin":124,"end":131},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"D020051"},{"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."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":132},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":132},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":39,"end":54},"obj":"gene:411"},{"id":"T1","span":{"begin":94,"end":123},"obj":"disease:C0026709"}],"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":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"20143913-0#39#54#gene411","span":{"begin":39,"end":54},"obj":"gene411"},{"id":"20143913-0#94#123#diseaseC0026709","span":{"begin":94,"end":123},"obj":"diseaseC0026709"}],"relations":[{"id":"39#54#gene41194#123#diseaseC0026709","pred":"associated_with","subj":"20143913-0#39#54#gene411","obj":"20143913-0#94#123#diseaseC0026709"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":94,"end":123},"obj":"ORDO:583"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient."}