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PubMed:16434322 JSONTXT 10 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-122 Sentence denotes Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene.
T1 0-122 Sentence denotes Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene.
TextSentencer_T2 123-253 Sentence denotes Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder, affecting approximately 1 in 3,500 individuals worldwide.
T2 123-253 Sentence denotes Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder, affecting approximately 1 in 3,500 individuals worldwide.
TextSentencer_T3 254-364 Sentence denotes Mutations of the NF1 tumor suppressor gene predispose individuals to a variety of benign and malignant tumors.
T3 254-364 Sentence denotes Mutations of the NF1 tumor suppressor gene predispose individuals to a variety of benign and malignant tumors.
TextSentencer_T4 365-479 Sentence denotes Rhabdomyosarcoma (RMS) is an uncommon malignant soft tissue sarcoma and is also a rare tumor type in NF1 patients.
T4 365-479 Sentence denotes Rhabdomyosarcoma (RMS) is an uncommon malignant soft tissue sarcoma and is also a rare tumor type in NF1 patients.
TextSentencer_T5 480-516 Sentence denotes We report two cases of NF1 with RMS.
T5 480-516 Sentence denotes We report two cases of NF1 with RMS.
TextSentencer_T6 517-655 Sentence denotes The first is that of an infant with overlapping phenotypic features of NF1 and Noonan syndrome (NS) who presented with RMS of the bladder.
T6 517-655 Sentence denotes The first is that of an infant with overlapping phenotypic features of NF1 and Noonan syndrome (NS) who presented with RMS of the bladder.
TextSentencer_T7 656-747 Sentence denotes The second infant likewise exhibited NF1 features and was also associated with bladder RMS.
T7 656-747 Sentence denotes The second infant likewise exhibited NF1 features and was also associated with bladder RMS.
TextSentencer_T8 748-822 Sentence denotes DNA samples were extracted from peripheral blood and tumor tissue samples.
T8 748-822 Sentence denotes DNA samples were extracted from peripheral blood and tumor tissue samples.
TextSentencer_T9 823-1058 Sentence denotes We performed loss of heterozygosity (LOH) analysis of the NF1 gene by using seven intragenic markers (IVS27AAAT2.1, IVS27EVI-20, IVS27AC24.8, IVS27AC28.4, M98509, IVS27AC33.1, IVS38TG53.0) and one extragenic polymorphic marker (3'NF1).
T9 823-1058 Sentence denotes We performed loss of heterozygosity (LOH) analysis of the NF1 gene by using seven intragenic markers (IVS27AAAT2.1, IVS27EVI-20, IVS27AC24.8, IVS27AC28.4, M98509, IVS27AC33.1, IVS38TG53.0) and one extragenic polymorphic marker (3'NF1).
TextSentencer_T10 1059-1165 Sentence denotes A large deletion was detected in the NF1 gene in the NF1-Noonan syndrome (NF-NS) case associated with RMS.
T10 1059-1165 Sentence denotes A large deletion was detected in the NF1 gene in the NF1-Noonan syndrome (NF-NS) case associated with RMS.