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PubMed:119407 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-75 Sentence denotes Myeloproliferative disease of childhood associated with a trisomy 21 clone.
TextSentencer_T2 76-192 Sentence denotes Myeloproliferative disease of childhood is frequently associated with chromosomal anomalies, usually of the C group.
TextSentencer_T3 193-281 Sentence denotes Clinical features are similar to those of the juvenile type of chronic myeloid leukemia.
TextSentencer_T4 282-321 Sentence denotes A child with this disease is described.
TextSentencer_T5 322-491 Sentence denotes Marked myeloid proliferation, anemia, thrombocytopenia and hepatosplenomegaly were present; leukocyte alkaline phosphatase and fetal hemoglobin were moderately elevated.
TextSentencer_T6 492-570 Sentence denotes Chromosome analysis of bone marrow cells revealed a mosaicism 47,XX,+21/46,XX.
TextSentencer_T7 571-661 Sentence denotes Down's syndrome was ruled out by the child's normal phenotype and dermatoglyphic analysis.
TextSentencer_T8 662-757 Sentence denotes The cytogenetic finding is probably evidence for the clonal origin of the trisomy 21 cell line.
T1 0-75 Sentence denotes Myeloproliferative disease of childhood associated with a trisomy 21 clone.
T2 76-192 Sentence denotes Myeloproliferative disease of childhood is frequently associated with chromosomal anomalies, usually of the C group.
T3 193-281 Sentence denotes Clinical features are similar to those of the juvenile type of chronic myeloid leukemia.
T4 282-321 Sentence denotes A child with this disease is described.
T5 322-491 Sentence denotes Marked myeloid proliferation, anemia, thrombocytopenia and hepatosplenomegaly were present; leukocyte alkaline phosphatase and fetal hemoglobin were moderately elevated.
T6 492-570 Sentence denotes Chromosome analysis of bone marrow cells revealed a mosaicism 47,XX,+21/46,XX.
T7 571-661 Sentence denotes Down's syndrome was ruled out by the child's normal phenotype and dermatoglyphic analysis.
T8 662-757 Sentence denotes The cytogenetic finding is probably evidence for the clonal origin of the trisomy 21 cell line.

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 515-526 http://purl.obolibrary.org/obo/UBERON_0002371 denotes bone marrow

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 264-280 HP:0012324 denotes myeloid leukemia
AB2 352-358 HP:0001903 denotes anemia
AB3 360-376 HP:0001873 denotes thrombocytopenia
AB4 381-399 HP:0001433 denotes hepatosplenomegaly

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 515-526 http://purl.obolibrary.org/obo/UBERON_0002371 denotes bone marrow

PubCasesORDO

Id Subject Object Predicate Lexical cue
TI1 58-68 ORDO:870 denotes trisomy 21
AB1 256-280 ORDO:521 denotes chronic myeloid leukemia
AB2 736-746 ORDO:870 denotes trisomy 21