PubMed:15033202 / 91-354 JSONTXT

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{"project":"LitCoin-sentences","denotations":[{"id":"T2","span":{"begin":0,"end":263},"obj":"Sentence"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin_Mondo","denotations":[{"id":"T3","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":36,"end":40},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":137,"end":147},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0009623"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0021136"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0021140"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0001149"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T2","span":{"begin":22,"end":30},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":36,"end":40},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":111,"end":116},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":117,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":162,"end":178},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":217,"end":221},"obj":"GeneOrGeneProduct"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T2","span":{"begin":22,"end":30},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":36,"end":40},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":111,"end":116},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":117,"end":123},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":162,"end":178},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":217,"end":221},"obj":"GeneOrGeneProduct"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T3","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":61,"end":84},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":250,"end":262},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"originalLabel","subj":"T3","obj":"D049932"},{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D043171"},{"id":"A5","pred":"originalLabel","subj":"T5","obj":"D008831"},{"id":"A6","pred":"originalLabel","subj":"T6","obj":"D009369"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T2","span":{"begin":4,"end":30},"obj":"GeneOrGeneProduct"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin_Mondo_095","denotations":[{"id":"T3","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":162,"end":178},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0009623"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0001149"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0021094"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T3","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":61,"end":84},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":117,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":162,"end":178},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":250,"end":262},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"ID:","subj":"T3","obj":"D049932"},{"id":"A4","pred":"ID:","subj":"T4","obj":"D043171"},{"id":"A5","pred":"ID:","subj":"T5","obj":"DISEASE"},{"id":"A6","pred":"ID:","subj":"T6","obj":"D008831"},{"id":"A7","pred":"ID:","subj":"T7","obj":"DISEASE"},{"id":"A8","pred":"ID:","subj":"T8","obj":"D009369"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T3","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":61,"end":84},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":117,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":162,"end":178},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T8","span":{"begin":250,"end":262},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A3","pred":"#label","subj":"T3","obj":"D049932"},{"id":"A4","pred":"#label","subj":"T4","obj":"D043171"},{"id":"A5","pred":"#label","subj":"T5","obj":"DISEASE"},{"id":"A6","pred":"#label","subj":"T6","obj":"D008831"},{"id":"A7","pred":"#label","subj":"T7","obj":"DISEASE"},{"id":"A8","pred":"#label","subj":"T8","obj":"D009369"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}

{"project":"LitCoin-training-merged","denotations":[{"id":"T2","span":{"begin":4,"end":30},"obj":"GeneOrGeneProduct"},{"id":"T13360","span":{"begin":250,"end":262},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T23922","span":{"begin":162,"end":178},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T84434","span":{"begin":148,"end":160},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T925","span":{"begin":117,"end":135},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2738","span":{"begin":61,"end":84},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T83827","span":{"begin":4,"end":30},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T13360","obj":"D009369"},{"id":"A7","pred":"#label","subj":"T23922","obj":"DISEASE"},{"id":"A6","pred":"#label","subj":"T84434","obj":"D008831"},{"id":"A5","pred":"#label","subj":"T925","obj":"DISEASE"},{"id":"A4","pred":"#label","subj":"T2738","obj":"D043171"},{"id":"A3","pred":"#label","subj":"T83827","obj":"D049932"}],"text":"The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized by early growth retardation, congenital microcephaly, immunodeficiency, borderline mental development, and a high tendency to lymphoreticular malignancies."}