> top > projects > sentences > docs > PubMed:10102532 > annotations
sentences Home  

PubMed:10102532 JSONTXT 9 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-73 Sentence denotes von Willebrand disease with G4022A mutation (vWd Sungnam): a case report.
T1 0-73 Sentence denotes von Willebrand disease with G4022A mutation (vWd Sungnam): a case report.
TextSentencer_T2 74-234 Sentence denotes A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies.
T2 74-234 Sentence denotes A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members were investigated by hemostatic and molecular genetic studies.
TextSentencer_T3 235-527 Sentence denotes The propositus, who experienced frequent bleeding episodes, was characterized by a normal level of von Willebrand factor (vWF) antigen (54%), reduced vWF ristocetin cofactor activity (5%), decreased factor VIII clotting activity (25%) and absent high molecular weight multimers in the plasma.
T3 235-527 Sentence denotes The propositus, who experienced frequent bleeding episodes, was characterized by a normal level of von Willebrand factor (vWF) antigen (54%), reduced vWF ristocetin cofactor activity (5%), decreased factor VIII clotting activity (25%) and absent high molecular weight multimers in the plasma.
TextSentencer_T4 528-638 Sentence denotes An exon 28 fragment coding for the A1 and A2 domains was amplified by polymerase chain reaction and sequenced.
T4 528-638 Sentence denotes An exon 28 fragment coding for the A1 and A2 domains was amplified by polymerase chain reaction and sequenced.
TextSentencer_T5 639-777 Sentence denotes We found a heterozygous mutation (G4022A), producing an additional PstI restriction site, which resulted in the substitution of Arg578Gln.
T5 639-777 Sentence denotes We found a heterozygous mutation (G4022A), producing an additional PstI restriction site, which resulted in the substitution of Arg578Gln.
TextSentencer_T6 778-903 Sentence denotes Family studies, including the parents and a brother, were negative for this mutation and vWF abnormalities were not observed.
T6 778-903 Sentence denotes Family studies, including the parents and a brother, were negative for this mutation and vWF abnormalities were not observed.
TextSentencer_T7 904-1069 Sentence denotes We confirmed that G to A mutation in the region of the platelet glycoprotein Ib binding domain of vWF causes the qualitative type 2 defect in von Willebrand disease.
T7 904-1069 Sentence denotes We confirmed that G to A mutation in the region of the platelet glycoprotein Ib binding domain of vWF causes the qualitative type 2 defect in von Willebrand disease.