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PubMed:119407 JSONTXT 7 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-75 Sentence denotes Myeloproliferative disease of childhood associated with a trisomy 21 clone.
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.
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.
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.
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.
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.
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.
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.
T8 662-757 Sentence denotes The cytogenetic finding is probably evidence for the clonal origin of the trisomy 21 cell line.