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PubMed:18363941 JSONTXT

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PubMed_ArguminSci

Id Subject Object Predicate Lexical cue
T1 46-75 DRI_Background denotes Kufs' disease (adult neuronal
T2 97-205 DRI_Background denotes ) is a rare form of neurodegenerative lysosomal storage disease, the genetic basis of which remains obscure.
T3 206-428 DRI_Challenge denotes We present a case of a 53-year-old man with a long history of adult onset epilepsy who presented with confusion and amnesia, and subsequently underwent rapidly progressive cognitive decline associated with myoclonic jerks.
T4 429-482 DRI_Background denotes The clinical diagnosis was Creutzfeldt Jakob disease.
T5 483-573 DRI_Background denotes However, autopsy brain examination revealed changes of Kufs' disease (Adult onset neuronal
T6 595-626 DRI_Background denotes , or ANCL, also known as CLN4).
T7 627-825 DRI_Outcome denotes No specific gross abnormalities were found but light microscopic examination revealed widespread neuronal ballooning and histochemical staining showed neuronal accumulation of PAS-positive material.
T8 826-931 DRI_Outcome denotes Ultrastructural examination demonstrated excessive and abnormal lipopigment lysosomes typical of neuronal
T9 953-954 DRI_Outcome denotes .
T10 955-1069 DRI_Outcome denotes The typical clinical and pathologic features of the Kufs' disease are discussed and the classification of neuronal
T11 1092-1104 DRI_Outcome denotes is reviewed.

PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 46-59 DiseaseOrPhenotypicFeature denotes Kufs' disease 0019260
T2 61-97 DiseaseOrPhenotypicFeature denotes adult neuronal ceroid lipofuscinosis 0019260
T3 135-160 DiseaseOrPhenotypicFeature denotes lysosomal storage disease 0002561
T4 280-288 DiseaseOrPhenotypicFeature denotes epilepsy 0005027
T5 322-329 DiseaseOrPhenotypicFeature denotes amnesia 0001152
T6 456-481 DiseaseOrPhenotypicFeature denotes Creutzfeldt Jakob disease 0005357
T7 538-551 DiseaseOrPhenotypicFeature denotes Kufs' disease 0019260
T8 565-595 DiseaseOrPhenotypicFeature denotes neuronal ceroid lipofuscinosis 0016295
T9 600-604 DiseaseOrPhenotypicFeature denotes ANCL 0019260
T10 803-806 DiseaseOrPhenotypicFeature denotes PAS 0004277
T11 923-953 DiseaseOrPhenotypicFeature denotes neuronal ceroid lipofuscinosis 0016295
T12 1007-1020 DiseaseOrPhenotypicFeature denotes Kufs' disease 0019260
T13 1061-1091 DiseaseOrPhenotypicFeature denotes neuronal ceroid lipofuscinosis 0016295

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-45 Sentence denotes 53-year-old man with rapid cognitive decline.
TextSentencer_T2 46-205 Sentence denotes Kufs' disease (adult neuronal ceroid lipofuscinosis) is a rare form of neurodegenerative lysosomal storage disease, the genetic basis of which remains obscure.
TextSentencer_T3 206-428 Sentence denotes We present a case of a 53-year-old man with a long history of adult onset epilepsy who presented with confusion and amnesia, and subsequently underwent rapidly progressive cognitive decline associated with myoclonic jerks.
TextSentencer_T4 429-482 Sentence denotes The clinical diagnosis was Creutzfeldt Jakob disease.
TextSentencer_T5 483-626 Sentence denotes However, autopsy brain examination revealed changes of Kufs' disease (Adult onset neuronal ceroid lipofuscinosis, or ANCL, also known as CLN4).
TextSentencer_T6 627-825 Sentence denotes No specific gross abnormalities were found but light microscopic examination revealed widespread neuronal ballooning and histochemical staining showed neuronal accumulation of PAS-positive material.
TextSentencer_T7 826-954 Sentence denotes Ultrastructural examination demonstrated excessive and abnormal lipopigment lysosomes typical of neuronal ceroid lipofuscinosis.
TextSentencer_T8 955-1104 Sentence denotes The typical clinical and pathologic features of the Kufs' disease are discussed and the classification of neuronal ceroid lipofuscinosis is reviewed.
T1 0-45 Sentence denotes 53-year-old man with rapid cognitive decline.
T2 46-205 Sentence denotes Kufs' disease (adult neuronal ceroid lipofuscinosis) is a rare form of neurodegenerative lysosomal storage disease, the genetic basis of which remains obscure.
T3 206-428 Sentence denotes We present a case of a 53-year-old man with a long history of adult onset epilepsy who presented with confusion and amnesia, and subsequently underwent rapidly progressive cognitive decline associated with myoclonic jerks.
T4 429-482 Sentence denotes The clinical diagnosis was Creutzfeldt Jakob disease.
T5 483-626 Sentence denotes However, autopsy brain examination revealed changes of Kufs' disease (Adult onset neuronal ceroid lipofuscinosis, or ANCL, also known as CLN4).
T6 627-825 Sentence denotes No specific gross abnormalities were found but light microscopic examination revealed widespread neuronal ballooning and histochemical staining showed neuronal accumulation of PAS-positive material.
T7 826-954 Sentence denotes Ultrastructural examination demonstrated excessive and abnormal lipopigment lysosomes typical of neuronal ceroid lipofuscinosis.
T8 955-1104 Sentence denotes The typical clinical and pathologic features of the Kufs' disease are discussed and the classification of neuronal ceroid lipofuscinosis is reviewed.

PubCasesHPO

Id Subject Object Predicate Lexical cue
AB1 308-317 HP:0001289 denotes confusion

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 67-75 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T2 565-573 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T3 724-732 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T4 778-786 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T5 923-931 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T6 1061-1069 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal
PD-UBERON-AE-B_T7 500-505 http://purl.obolibrary.org/obo/UBERON_0000955 denotes brain

PubCasesORDO

Id Subject Object Predicate Lexical cue
AB1 46-59 ORDO:79262 denotes Kufs' disease
AB2 61-97 ORDO:79262 denotes adult neuronal ceroid lipofuscinosis
AB3 538-551 ORDO:79262 denotes Kufs' disease
AB4 600-604 ORDO:79262 denotes ANCL
AB5 1007-1020 ORDO:79262 denotes Kufs' disease

UBERON-AE

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 500-505 http://purl.obolibrary.org/obo/UBERON_0000955 denotes brain