PubMed:22669887 JSON TXT 17 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id	Subject	Object	Predicate	Lexical cue
TextSentencer_T1	0-106	Sentence	denotes	Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.
T1	0-106	Sentence	denotes	Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.
TextSentencer_T2	107-215	Sentence	denotes	The authors report a case of purine nucleoside phosphorylase (PNP) deficiency for the first time from India.
T2	107-215	Sentence	denotes	The authors report a case of purine nucleoside phosphorylase (PNP) deficiency for the first time from India.
TextSentencer_T3	216-343	Sentence	denotes	The case presented with recurrent severe infections, developmental delays, seizures and progressive neurological deterioration.
T3	216-343	Sentence	denotes	The case presented with recurrent severe infections, developmental delays, seizures and progressive neurological deterioration.
TextSentencer_T4	344-480	Sentence	denotes	The diagnosis of primary immunodeficiency disorder was delayed in spite of recurrent infection due to predominant neurological symptoms.
T4	344-480	Sentence	denotes	The diagnosis of primary immunodeficiency disorder was delayed in spite of recurrent infection due to predominant neurological symptoms.
TextSentencer_T5	481-570	Sentence	denotes	Sequencing of the PNP gene revealed a novel mutation resulting in a premature stop codon.
T5	481-570	Sentence	denotes	Sequencing of the PNP gene revealed a novel mutation resulting in a premature stop codon.