PubMed:16361247 / 0-274 JSONTXT

{"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 (neuraminida"}

{"project":"uniprot-human","denotations":[{"id":"T1","span":{"begin":242,"end":261},"obj":"http://www.uniprot.org/uniprot/Q99519"}],"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 (neuraminida"}

{"project":"uniprot-mouse","denotations":[{"id":"T1","span":{"begin":242,"end":261},"obj":"http://www.uniprot.org/uniprot/O35657"}],"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 (neuraminida"}

{"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"}],"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 (neuraminida"}

{"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"}],"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 (neuraminida"}

{"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"}],"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 (neuraminida"}

{"project":"EDAM-DFO","denotations":[{"id":"T1","span":{"begin":100,"end":106},"obj":"http://edamontology.org/operation_3435"}],"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 (neuraminida"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16361247-1#97#116#gene4758","span":{"begin":242,"end":261},"obj":"gene4758"},{"id":"16361247-1#0#10#diseaseC0026697","span":{"begin":145,"end":155},"obj":"diseaseC0026697"},{"id":"16361247-1#0#10#diseaseC0268226","span":{"begin":145,"end":155},"obj":"diseaseC0268226"},{"id":"16361247-1#15#32#diseaseC0268233","span":{"begin":160,"end":177},"obj":"diseaseC0268233"},{"id":"16361247-1#15#32#diseaseC0268233","span":{"begin":160,"end":177},"obj":"diseaseC0268233"},{"id":"16361247-1#15#32#diseaseC0268233","span":{"begin":160,"end":177},"obj":"diseaseC0268233"},{"id":"16361247-1#37#63#diseaseC0085078","span":{"begin":182,"end":208},"obj":"diseaseC0085078"},{"id":"16361247-1#15#32#diseaseC0268233","span":{"begin":160,"end":177},"obj":"diseaseC0268233"},{"id":"16361247-1#37#63#diseaseC0085078","span":{"begin":182,"end":208},"obj":"diseaseC0085078"}],"relations":[{"id":"97#116#gene47580#10#diseaseC0026697","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#0#10#diseaseC0026697"},{"id":"97#116#gene47580#10#diseaseC0268226","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#0#10#diseaseC0268226"},{"id":"97#116#gene475815#32#diseaseC0268233","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#15#32#diseaseC0268233"},{"id":"97#116#gene475815#32#diseaseC0268233","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#15#32#diseaseC0268233"},{"id":"97#116#gene475815#32#diseaseC0268233","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#15#32#diseaseC0268233"},{"id":"97#116#gene475837#63#diseaseC0085078","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#37#63#diseaseC0085078"},{"id":"97#116#gene475815#32#diseaseC0268233","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#15#32#diseaseC0268233"},{"id":"97#116#gene475837#63#diseaseC0085078","pred":"associated_with","subj":"16361247-1#97#116#gene4758","obj":"16361247-1#37#63#diseaseC0085078"}],"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 (neuraminida"}

{"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":"T7","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T9","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T11","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T13","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T19","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T23","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T27","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T29","span":{"begin":182,"end":208},"obj":"disease:C0085078"},{"id":"T33","span":{"begin":160,"end":177},"obj":"disease:C0268233"},{"id":"T35","span":{"begin":182,"end":208},"obj":"disease:C0085078"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"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 (neuraminida"}

{"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"}],"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"}],"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 (neuraminida"}

{"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 (neuraminida"}

{"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 (neuraminida"}

{"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 (neuraminida"}