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PubMed:12626384 / 128-411 JSONTXT

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sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T2 0-105 Sentence denotes Fabry disease is a lysosomal storage disease arising from deficiency of the enzyme alpha-galactosidase A.
TextSentencer_T3 106-283 Sentence denotes Two recombinant protein therapeutics, Fabrazyme (agalsidase beta) and Replagal (agalsidase alfa), have been approved in Europe as enzyme replacement therapies for Fabry disease.
T2 0-283 Sentence denotes Fabry disease is a lysosomal storage disease arising from deficiency of the enzyme alpha-galactosidase A. Two recombinant protein therapeutics, Fabrazyme (agalsidase beta) and Replagal (agalsidase alfa), have been approved in Europe as enzyme replacement therapies for Fabry disease.
T2 0-105 Sentence denotes Fabry disease is a lysosomal storage disease arising from deficiency of the enzyme alpha-galactosidase A.
T3 106-283 Sentence denotes Two recombinant protein therapeutics, Fabrazyme (agalsidase beta) and Replagal (agalsidase alfa), have been approved in Europe as enzyme replacement therapies for Fabry disease.

GlycoBiology-FMA

Id Subject Object Predicate Lexical cue
_T3 19-28 FMAID:63836 denotes lysosomal
_T4 19-28 FMAID:162299 denotes lysosomal
_T5 89-102 FMAID:196789 denotes galactosidase
_T6 89-102 FMAID:82794 denotes galactosidase
_T7 122-129 FMAID:67257 denotes protein
_T8 122-129 FMAID:165447 denotes protein

uniprot-human

Id Subject Object Predicate Lexical cue
T1 83-104 http://www.uniprot.org/uniprot/P06280 denotes alpha-galactosidase A
T2 155-165 http://www.uniprot.org/uniprot/P06280 denotes agalsidase
T3 186-196 http://www.uniprot.org/uniprot/P06280 denotes agalsidase

uniprot-mouse

Id Subject Object Predicate Lexical cue
T1 83-104 http://www.uniprot.org/uniprot/P51569 denotes alpha-galactosidase A

GlycoBiology-NCBITAXON

Id Subject Object Predicate Lexical cue
T1 166-170 http://purl.bioontology.org/ontology/NCBITAXON/3554 denotes beta
T2 166-170 http://purl.bioontology.org/ontology/NCBITAXON/158455 denotes beta

GO-BP

Id Subject Object Predicate Lexical cue
T2 29-36 http://purl.obolibrary.org/obo/GO_0051235 denotes storage
T4 29-36 http://purl.obolibrary.org/obo/GO_0035732 denotes storage
T5 83-102 http://purl.obolibrary.org/obo/GO_0004557 denotes alpha-galactosidase

GO-CC

Id Subject Object Predicate Lexical cue
T1 19-28 http://purl.obolibrary.org/obo/GO_0005764 denotes lysosomal

EDAM-topics

Id Subject Object Predicate Lexical cue
T3 6-13 http://edamontology.org/topic_0634 denotes disease
T4 19-28 http://edamontology.org/topic_0616 denotes lysosomal
T5 37-44 http://edamontology.org/topic_0634 denotes disease
T6 122-129 http://edamontology.org/topic_0078 denotes protein
T7 275-282 http://edamontology.org/topic_0634 denotes disease

EDAM-DFO

Id Subject Object Predicate Lexical cue
T2 122-129 http://edamontology.org/format_1208 denotes protein
T3 122-129 http://edamontology.org/data_1467 denotes protein

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
12626384-1#83#104#gene2717 83-104 gene2717 denotes alpha-galactosidase A
12626384-1#0#13#diseaseC0002986 0-13 diseaseC0002986 denotes Fabry disease
12626384-1#19#44#diseaseC0085078 19-44 diseaseC0085078 denotes lysosomal storage disease
83#104#gene27170#13#diseaseC0002986 12626384-1#83#104#gene2717 12626384-1#0#13#diseaseC0002986 associated_with alpha-galactosidase A,Fabry disease
83#104#gene271719#44#diseaseC0085078 12626384-1#83#104#gene2717 12626384-1#19#44#diseaseC0085078 associated_with alpha-galactosidase A,lysosomal storage disease

DisGeNET

Id Subject Object Predicate Lexical cue
T0 83-104 gene:2717 denotes alpha-galactosidase A
T1 0-13 disease:C0002986 denotes Fabry disease
T2 83-104 gene:2717 denotes alpha-galactosidase A
T3 19-44 disease:C0085078 denotes lysosomal storage disease
R1 T0 T1 associated_with alpha-galactosidase A,Fabry disease
R2 T2 T3 associated_with alpha-galactosidase A,lysosomal storage disease

mondo_disease

Id Subject Object Predicate Lexical cue mondo_id
T2 0-13 Disease denotes Fabry disease http://purl.obolibrary.org/obo/MONDO_0010526
T3 19-44 Disease denotes lysosomal storage disease http://purl.obolibrary.org/obo/MONDO_0002561
T4 269-282 Disease denotes Fabry disease http://purl.obolibrary.org/obo/MONDO_0010526