> top > projects > sentences > docs > PubMed:999542 > annotations
sentences Home  

PubMed:999542 JSONTXT 6 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-16 Sentence denotes Hartnup disease.
T1 0-16 Sentence denotes Hartnup disease.
TextSentencer_T2 17-70 Sentence denotes Clinical, pathological, and biochemical observations.
T2 17-70 Sentence denotes Clinical, pathological, and biochemical observations.
TextSentencer_T3 71-203 Sentence denotes Hartnup disease is a rare genetic disorder of amino acid transport associated with variable and intermittent clinical abnormalities.
T3 71-203 Sentence denotes Hartnup disease is a rare genetic disorder of amino acid transport associated with variable and intermittent clinical abnormalities.
TextSentencer_T4 204-376 Sentence denotes A family is described in which three siblings had an intermittently progressive neurological disease and two of the affected siblings had the Hartnup-pattern aminoaciduria.
T4 204-376 Sentence denotes A family is described in which three siblings had an intermittently progressive neurological disease and two of the affected siblings had the Hartnup-pattern aminoaciduria.
TextSentencer_T5 377-532 Sentence denotes Neuropathological examination of one case showed severe diffuse atrophy, generalized neuronal loss in the cortex, and Purkinje cell loss in the cerebellum.
T5 377-532 Sentence denotes Neuropathological examination of one case showed severe diffuse atrophy, generalized neuronal loss in the cortex, and Purkinje cell loss in the cerebellum.
TextSentencer_T6 533-858 Sentence denotes In vivo and in vitro studies of intestinal amino acid transport in the surviving sibling indicated a partial defect in the transport of several neutral amino acids (tryptophan, alanine, serine, and methionine) with normal transport of other neutral amino acids (threonine, phenylalanine, histidine, tyrosine, and isoleucine).
T6 533-858 Sentence denotes In vivo and in vitro studies of intestinal amino acid transport in the surviving sibling indicated a partial defect in the transport of several neutral amino acids (tryptophan, alanine, serine, and methionine) with normal transport of other neutral amino acids (threonine, phenylalanine, histidine, tyrosine, and isoleucine).
TextSentencer_T7 859-948 Sentence denotes Transport of glycine, proline, hydroxyproline, and the basic amino acids appeared normal.
T7 859-948 Sentence denotes Transport of glycine, proline, hydroxyproline, and the basic amino acids appeared normal.