PubMed:7811247 / 465-782 JSONTXT

{"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T8","span":{"begin":62,"end":65},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":71,"end":92},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":280,"end":283},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"D000326"},{"id":"A9","pred":"#label","subj":"T9","obj":"D000326"},{"id":"A10","pred":"#label","subj":"T10","obj":"D000326"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"TEST-ChemicalEntity","denotations":[{"id":"T10","span":{"begin":168,"end":190},"obj":"ChemicalEntity"}],"attributes":[{"id":"A10","pred":"ID:","subj":"T10","obj":"http://purl.obolibrary.org/obo/CHEBI_15904"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"TEST-OrganismTaxon","denotations":[{"id":"T2","span":{"begin":29,"end":36},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":284,"end":292},"obj":"OrganismTaxon"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"Test-GeneOrGeneProduct","denotations":[{"id":"T1","span":{"begin":168,"end":190},"obj":"GeneOrGeneProduct"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"Test-merged-2","denotations":[{"id":"T25434","span":{"begin":168,"end":190},"obj":"ChemicalEntity"},{"id":"T88141","span":{"begin":168,"end":190},"obj":"GeneOrGeneProduct"},{"id":"T29740","span":{"begin":29,"end":36},"obj":"OrganismTaxon"},{"id":"T18858","span":{"begin":284,"end":292},"obj":"OrganismTaxon"},{"id":"T8","span":{"begin":62,"end":65},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":71,"end":92},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T10","span":{"begin":280,"end":283},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A63145","pred":"ID:","subj":"T25434","obj":"http://purl.obolibrary.org/obo/CHEBI_15904"},{"id":"A8","pred":"#label","subj":"T8","obj":"D000326"},{"id":"A9","pred":"#label","subj":"T9","obj":"D000326"},{"id":"A10","pred":"#label","subj":"T10","obj":"D000326"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":317},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":317},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"PubCasesORDO","denotations":[{"id":"AB4","span":{"begin":62,"end":65},"obj":"ORDO:43"},{"id":"AB5","span":{"begin":280,"end":283},"obj":"ORDO:43"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"NCBIDiseaseCorpus","denotations":[{"id":"T8","span":{"begin":53,"end":65},"obj":"SpecificDisease:D000326"},{"id":"T9","span":{"begin":71,"end":92},"obj":"SpecificDisease:D000326"},{"id":"T10","span":{"begin":98,"end":110},"obj":"SpecificDisease:D000224"},{"id":"T11","span":{"begin":280,"end":283},"obj":"Modifier:D000326"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"testtesttest","denotations":[{"id":"T8","span":{"begin":53,"end":65},"obj":"SpecificDisease:D000326"},{"id":"T9","span":{"begin":71,"end":92},"obj":"SpecificDisease:D000326"},{"id":"T10","span":{"begin":98,"end":110},"obj":"SpecificDisease:D000224"},{"id":"T11","span":{"begin":280,"end":283},"obj":"Modifier:D000326"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}

{"project":"NCBI-Disease-Train","denotations":[{"id":"T250","span":{"begin":53,"end":65},"obj":"SpecificDisease"},{"id":"T251","span":{"begin":71,"end":92},"obj":"SpecificDisease"},{"id":"T252","span":{"begin":98,"end":110},"obj":"SpecificDisease"},{"id":"T253","span":{"begin":280,"end":283},"obj":"Modifier"}],"attributes":[{"id":"A250","pred":"database_id","subj":"T250","obj":"D000326"},{"id":"A251","pred":"database_id","subj":"T251","obj":"D000326"},{"id":"A252","pred":"database_id","subj":"T252","obj":"D000224"},{"id":"A253","pred":"database_id","subj":"T253","obj":"D000326"}],"text":"Five of nine siblings of the patient, comprising two cerebral ALD, one adrenomyeloneuropathy, one Addison only as well as the symptomatic mother (all accumulating very long chain fatty acids) carried this mutation, which was not found in the unaffected persons, in five unrelated ALD patients, and in twenty controls."}