PubMed:12626384 / 128-411
Annnotations
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 |