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PubMed:999542 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-16 Sentence denotes Hartnup disease.
TextSentencer_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.
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.
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.
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).
TextSentencer_T7 859-948 Sentence denotes Transport of glycine, proline, hydroxyproline, and the basic amino acids appeared normal.
T1 0-16 Sentence denotes Hartnup disease.
T2 17-70 Sentence denotes Clinical, pathological, and biochemical observations.
T3 71-203 Sentence denotes Hartnup disease is a rare genetic disorder of amino acid transport associated with variable and intermittent clinical abnormalities.
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.
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.
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).
T7 859-948 Sentence denotes Transport of glycine, proline, hydroxyproline, and the basic amino acids appeared normal.

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 362-375 HP:0003355 denotes aminoaciduria

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 483-489 http://purl.obolibrary.org/obo/UBERON_0001851 denotes cortex
PD-UBERON-AE-B_T2 521-531 http://purl.obolibrary.org/obo/UBERON_0002037 denotes cerebellum
PD-UBERON-AE-B_T3 565-575 http://purl.obolibrary.org/obo/UBERON_0000160 denotes intestinal

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 71-86 ORDO:2116 denotes Hartnup disease

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 462-470 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T2 483-489 http://purl.obolibrary.org/obo/UBERON_0001851 denotes cortex
PD-UBERON-AE-B_T3 521-531 http://purl.obolibrary.org/obo/UBERON_0002037 denotes cerebellum
PD-UBERON-AE-B_T4 565-575 http://purl.obolibrary.org/obo/UBERON_0000160 denotes intestinal