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PubMed:14736728 / 113-252 JSONTXT

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GlyCosmos600-CLO

Id Subject Object Predicate Lexical cue
T1 89-98 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal

ICD10

Id Subject Object Predicate Lexical cue
T1 15-45 http://purl.bioontology.org/ontology/ICD10/E75.4 denotes neuronal ceroid lipofuscinosis

GlycoBiology-FMA

Id Subject Object Predicate Lexical cue
_T5 15-23 FMAID:166033 denotes neuronal
_T6 15-23 FMAID:54527 denotes neuronal
_T7 15-23 FMAID:150783 denotes neuronal
_T8 89-98 FMAID:63836 denotes lysosomal
_T9 89-98 FMAID:162299 denotes lysosomal

uniprot-human

Id Subject Object Predicate Lexical cue
T1 99-122 http://www.uniprot.org/uniprot/O14773 denotes tripeptidyl peptidase-I

uniprot-mouse

Id Subject Object Predicate Lexical cue
T1 99-122 http://www.uniprot.org/uniprot/O89023 denotes tripeptidyl peptidase-I

GlycoBiology-NCBITAXON

Id Subject Object Predicate Lexical cue
T1 0-4 http://purl.bioontology.org/ontology/NCBITAXON/8186 denotes Late

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-139 Sentence denotes Late infantile neuronal ceroid lipofuscinosis (LINCL) is caused by the deficiency of the lysosomal tripeptidyl peptidase-I encoded by CLN2.
T2 0-139 Sentence denotes Late infantile neuronal ceroid lipofuscinosis (LINCL) is caused by the deficiency of the lysosomal tripeptidyl peptidase-I encoded by CLN2.

GO-CC

Id Subject Object Predicate Lexical cue
T1 89-98 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal

EDAM-topics

Id Subject Object Predicate Lexical cue
T4 89-98 http://edamontology.org/topic_0616 denotes lysosomal

GlyCosmos600-FMA

Id Subject Object Predicate Lexical cue fma_id
T2 89-98 Body_part denotes lysosomal http://purl.org/sig/ont/fma/fma63836

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
14736728-1#99#122#gene1200 99-122 gene1200 denotes tripeptidyl peptidase-I
14736728-1#134#138#gene1200 134-138 gene1200 denotes CLN2
14736728-1#0#45#diseaseC0022340 0-45 diseaseC0022340 denotes Late infantile neuronal ceroid lipofuscinosis
14736728-1#47#52#diseaseC0022340 47-52 diseaseC0022340 denotes LINCL
14736728-1#0#45#diseaseC0022340 0-45 diseaseC0022340 denotes Late infantile neuronal ceroid lipofuscinosis
14736728-1#47#52#diseaseC0022340 47-52 diseaseC0022340 denotes LINCL
99#122#gene12000#45#diseaseC0022340 14736728-1#99#122#gene1200 14736728-1#0#45#diseaseC0022340 associated_with tripeptidyl peptidase-I,Late infantile neuronal ceroid lipofuscinosis
99#122#gene120047#52#diseaseC0022340 14736728-1#99#122#gene1200 14736728-1#47#52#diseaseC0022340 associated_with tripeptidyl peptidase-I,LINCL
99#122#gene12000#45#diseaseC0022340 14736728-1#99#122#gene1200 14736728-1#0#45#diseaseC0022340 associated_with tripeptidyl peptidase-I,Late infantile neuronal ceroid lipofuscinosis
99#122#gene120047#52#diseaseC0022340 14736728-1#99#122#gene1200 14736728-1#47#52#diseaseC0022340 associated_with tripeptidyl peptidase-I,LINCL
134#138#gene12000#45#diseaseC0022340 14736728-1#134#138#gene1200 14736728-1#0#45#diseaseC0022340 associated_with CLN2,Late infantile neuronal ceroid lipofuscinosis
134#138#gene120047#52#diseaseC0022340 14736728-1#134#138#gene1200 14736728-1#47#52#diseaseC0022340 associated_with CLN2,LINCL
134#138#gene12000#45#diseaseC0022340 14736728-1#134#138#gene1200 14736728-1#0#45#diseaseC0022340 associated_with CLN2,Late infantile neuronal ceroid lipofuscinosis
134#138#gene120047#52#diseaseC0022340 14736728-1#134#138#gene1200 14736728-1#47#52#diseaseC0022340 associated_with CLN2,LINCL

pubmed-enju-pas

Id Subject Object Predicate Lexical cue
EnjuParser_T17 0-4 JJ denotes Late
EnjuParser_T18 5-14 JJ denotes infantile
EnjuParser_T19 15-23 JJ denotes neuronal
EnjuParser_T20 24-30 NN denotes ceroid
EnjuParser_T21 31-45 NN denotes lipofuscinosis
EnjuParser_T22 46-47 -LRB- denotes (
EnjuParser_T23 47-52 NN denotes LINCL
EnjuParser_T24 52-53 -RRB- denotes )
EnjuParser_T25 54-56 VBZ denotes is
EnjuParser_T26 57-63 VBN denotes caused
EnjuParser_T27 64-66 IN denotes by
EnjuParser_T28 67-70 DT denotes the
EnjuParser_T29 71-81 NN denotes deficiency
EnjuParser_T30 82-84 IN denotes of
EnjuParser_T31 85-88 DT denotes the
EnjuParser_T32 89-98 JJ denotes lysosomal
EnjuParser_T33 99-110 NN denotes tripeptidyl
EnjuParser_T34 111-122 NN denotes peptidase-I
EnjuParser_T35 123-130 VBN denotes encoded
EnjuParser_T36 131-133 IN denotes by
EnjuParser_T37 134-138 NN denotes CLN2
EnjuParser_R16 EnjuParser_T21 EnjuParser_T17 arg1Of lipofuscinosis,Late
EnjuParser_R17 EnjuParser_T21 EnjuParser_T18 arg1Of lipofuscinosis,infantile
EnjuParser_R18 EnjuParser_T21 EnjuParser_T19 arg1Of lipofuscinosis,neuronal
EnjuParser_R19 EnjuParser_T21 EnjuParser_T20 arg1Of lipofuscinosis,ceroid
EnjuParser_R20 EnjuParser_T21 EnjuParser_T22 arg1Of lipofuscinosis,(
EnjuParser_R21 EnjuParser_T23 EnjuParser_T22 arg2Of LINCL,(
EnjuParser_R22 EnjuParser_T24 EnjuParser_T22 arg3Of ),(
EnjuParser_R23 EnjuParser_T21 EnjuParser_T25 arg1Of lipofuscinosis,is
EnjuParser_R24 EnjuParser_T26 EnjuParser_T25 arg2Of caused,is
EnjuParser_R25 EnjuParser_T29 EnjuParser_T26 arg1Of deficiency,caused
EnjuParser_R26 EnjuParser_T21 EnjuParser_T26 arg2Of lipofuscinosis,caused
EnjuParser_R27 EnjuParser_T29 EnjuParser_T27 arg2Of deficiency,by
EnjuParser_R28 EnjuParser_T29 EnjuParser_T28 arg1Of deficiency,the
EnjuParser_R29 EnjuParser_T29 EnjuParser_T30 arg1Of deficiency,of
EnjuParser_R30 EnjuParser_T34 EnjuParser_T30 arg2Of peptidase-I,of
EnjuParser_R31 EnjuParser_T34 EnjuParser_T31 arg1Of peptidase-I,the
EnjuParser_R32 EnjuParser_T34 EnjuParser_T32 arg1Of peptidase-I,lysosomal
EnjuParser_R33 EnjuParser_T34 EnjuParser_T33 arg1Of peptidase-I,tripeptidyl
EnjuParser_R34 EnjuParser_T37 EnjuParser_T35 arg1Of CLN2,encoded
EnjuParser_R35 EnjuParser_T34 EnjuParser_T35 arg2Of peptidase-I,encoded
EnjuParser_R36 EnjuParser_T37 EnjuParser_T36 arg2Of CLN2,by

performance-test

Id Subject Object Predicate Lexical cue
PD-UBERON-AE-B_T1 15-23 http://purl.obolibrary.org/obo/UBERON_2000602 denotes neuronal

DisGeNET

Id Subject Object Predicate Lexical cue
T0 99-122 gene:1200 denotes tripeptidyl peptidase-I
T1 0-45 disease:C0022340 denotes Late infantile neuronal ceroid lipofuscinosis
T2 99-122 gene:1200 denotes tripeptidyl peptidase-I
T3 47-52 disease:C0022340 denotes LINCL
T4 134-138 gene:1200 denotes CLN2
T5 0-45 disease:C0022340 denotes Late infantile neuronal ceroid lipofuscinosis
T6 134-138 gene:1200 denotes CLN2
T7 47-52 disease:C0022340 denotes LINCL
R1 T0 T1 associated_with tripeptidyl peptidase-I,Late infantile neuronal ceroid lipofuscinosis
R2 T2 T3 associated_with tripeptidyl peptidase-I,LINCL
R3 T4 T5 associated_with CLN2,Late infantile neuronal ceroid lipofuscinosis
R4 T6 T7 associated_with CLN2,LINCL

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T1 0-45 Disease denotes Late infantile neuronal ceroid lipofuscinosis http://purl.obolibrary.org/obo/MONDO_0008769|http://purl.obolibrary.org/obo/MONDO_0015674
T3 47-52 Disease denotes LINCL http://purl.obolibrary.org/obo/MONDO_0008769

Glycosmos15-CL

Id Subject Object Predicate Lexical cue cl_id
T1 15-23 Cell denotes neuronal http://purl.obolibrary.org/obo/CL:0000540