PubMed:16361247 / 0-464 JSON TXT

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sentences

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":144},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":144},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":144},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

GlycoBiology-GDGDB

{"project":"GlycoBiology-GDGDB","denotations":[{"id":"_T1","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012"},{"id":"_T2","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013"},{"id":"_T3","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014"},{"id":"_T4","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015"},{"id":"_T5","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016"},{"id":"_T6","span":{"begin":280,"end":284},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017"},{"id":"_T7","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00012"},{"id":"_T8","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00013"},{"id":"_T9","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00014"},{"id":"_T10","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00015"},{"id":"_T11","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00016"},{"id":"_T12","span":{"begin":371,"end":375},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00017"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

uniprot-human

{"project":"uniprot-human","denotations":[{"id":"T1","span":{"begin":242,"end":261},"obj":"http://www.uniprot.org/uniprot/Q99519"},{"id":"T2","span":{"begin":280,"end":284},"obj":"http://www.uniprot.org/uniprot/Q99519"},{"id":"T3","span":{"begin":371,"end":375},"obj":"http://www.uniprot.org/uniprot/Q99519"},{"id":"T8","span":{"begin":290,"end":318},"obj":"http://www.uniprot.org/uniprot/P10619"},{"id":"T9","span":{"begin":332,"end":336},"obj":"http://www.uniprot.org/uniprot/P10619"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

uniprot-mouse

{"project":"uniprot-mouse","denotations":[{"id":"T1","span":{"begin":242,"end":261},"obj":"http://www.uniprot.org/uniprot/O35657"},{"id":"T2","span":{"begin":290,"end":318},"obj":"http://www.uniprot.org/uniprot/P16675"},{"id":"T3","span":{"begin":332,"end":336},"obj":"http://www.uniprot.org/uniprot/P16675"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

GO-BP

{"project":"GO-BP","denotations":[{"id":"T1","span":{"begin":192,"end":199},"obj":"http://purl.obolibrary.org/obo/GO_0051235"},{"id":"T2","span":{"begin":192,"end":199},"obj":"http://purl.obolibrary.org/obo/GO_0035732"},{"id":"T3","span":{"begin":441,"end":452},"obj":"http://purl.obolibrary.org/obo/GO_0032502"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

GO-CC

{"project":"GO-CC","denotations":[{"id":"T1","span":{"begin":182,"end":191},"obj":"http://purl.obolibrary.org/obo/GO_0005764"},{"id":"T2","span":{"begin":242,"end":251},"obj":"http://purl.obolibrary.org/obo/GO_0005764"},{"id":"T3","span":{"begin":290,"end":299},"obj":"http://purl.obolibrary.org/obo/GO_0005764"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

EDAM-topics

{"project":"EDAM-topics","denotations":[{"id":"T1","span":{"begin":182,"end":191},"obj":"http://edamontology.org/topic_0616"},{"id":"T2","span":{"begin":200,"end":208},"obj":"http://edamontology.org/topic_0634"},{"id":"T3","span":{"begin":223,"end":230},"obj":"http://edamontology.org/topic_3053"},{"id":"T4","span":{"begin":242,"end":251},"obj":"http://edamontology.org/topic_0616"},{"id":"T5","span":{"begin":290,"end":299},"obj":"http://edamontology.org/topic_0616"},{"id":"T6","span":{"begin":311,"end":318},"obj":"http://edamontology.org/topic_0078"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

EDAM-DFO

{"project":"EDAM-DFO","denotations":[{"id":"T1","span":{"begin":100,"end":106},"obj":"http://edamontology.org/operation_3435"},{"id":"T2","span":{"begin":300,"end":318},"obj":"http://edamontology.org/format_1219"},{"id":"T3","span":{"begin":311,"end":318},"obj":"http://edamontology.org/format_1208"},{"id":"T4","span":{"begin":311,"end":318},"obj":"http://edamontology.org/data_1467"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

DisGeNET5_gene_disease

DisGeNET

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":242,"end":261},"obj":"gene:4758"},{"id":"T1","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T2","span":{"begin":242,"end":261},"obj":"gene:4758"},{"id":"T3","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T4","span":{"begin":242,"end":261},"obj":"gene:4758"},{"id":"T5","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T6","span":{"begin":280,"end":284},"obj":"gene:4758"},{"id":"T7","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T8","span":{"begin":280,"end":284},"obj":"gene:51162"},{"id":"T9","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T10","span":{"begin":280,"end":284},"obj":"gene:4758"},{"id":"T11","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T12","span":{"begin":280,"end":284},"obj":"gene:51162"},{"id":"T13","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T14","span":{"begin":280,"end":284},"obj":"gene:4758"},{"id":"T15","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T16","span":{"begin":280,"end":284},"obj":"gene:51162"},{"id":"T17","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T18","span":{"begin":290,"end":318},"obj":"gene:5476"},{"id":"T19","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T20","span":{"begin":290,"end":318},"obj":"gene:5476"},{"id":"T21","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T22","span":{"begin":319,"end":330},"obj":"gene:5476"},{"id":"T23","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T25","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T27","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T29","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T31","span":{"begin":371,"end":386},"obj":"disease:C0268228"},{"id":"T33","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T35","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T36","span":{"begin":319,"end":330},"obj":"gene:5476"},{"id":"T37","span":{"begin":371,"end":386},"obj":"disease:C0268228"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"},{"id":"R4","pred":"associated_with","subj":"T6","obj":"T7"},{"id":"R5","pred":"associated_with","subj":"T8","obj":"T9"},{"id":"R6","pred":"associated_with","subj":"T10","obj":"T11"},{"id":"R7","pred":"associated_with","subj":"T12","obj":"T13"},{"id":"R8","pred":"associated_with","subj":"T14","obj":"T15"},{"id":"R9","pred":"associated_with","subj":"T16","obj":"T17"},{"id":"R10","pred":"associated_with","subj":"T18","obj":"T19"},{"id":"R11","pred":"associated_with","subj":"T20","obj":"T21"},{"id":"R12","pred":"associated_with","subj":"T22","obj":"T23"},{"id":"R19","pred":"associated_with","subj":"T36","obj":"T37"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

mondo_disease

{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":64,"end":74},"obj":"Disease"},{"id":"T2","span":{"begin":79,"end":96},"obj":"Disease"},{"id":"T3","span":{"begin":145,"end":155},"obj":"Disease"},{"id":"T4","span":{"begin":160,"end":177},"obj":"Disease"},{"id":"T5","span":{"begin":182,"end":208},"obj":"Disease"},{"id":"T6","span":{"begin":371,"end":386},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0017734"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0009737"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0017734"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0009737"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0009738"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

Lectin-Jamboree-Sentence

{"project":"Lectin-Jamboree-Sentence","blocks":[{"id":"T1","span":{"begin":0,"end":144},"obj":"Sentence"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

Anatomy-UBERON

{"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":47,"end":58},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL_0000057"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

CL-cell

{"project":"CL-cell","denotations":[{"id":"T1","span":{"begin":47,"end":58},"obj":"Cell"}],"attributes":[{"id":"A1","pred":"cl_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL:0000057"}],"text":"Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement.\nSialidosis and galactosialidosis are lysosomal storage diseases caused by the genetic defects of lysosomal sialidase (neuraminidase-1; NEU1) and lysosomal protective protein/cathepsin A (PPCA), respectively, associated with a NEU1 deficiency, excessive accumulation of sialylglycoconjugates, and development of progress"}

PubMed:16361247 / 0-464 JSONTXT

Annnotations TAB JSON ListView MergeView

PubMed:16361247 / 0-464 JSON TXT