PubMed:16377754 / 392-528 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":136},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":136},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":136},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":0,"end":21},"obj":"HP_0008155"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"ICD10","denotations":[{"id":"T1","span":{"begin":0,"end":21},"obj":"http://purl.bioontology.org/ontology/ICD10/E76.3"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"GO-BP","denotations":[{"id":"T10","span":{"begin":51,"end":58},"obj":"http://purl.obolibrary.org/obo/GO_0051235"},{"id":"T11","span":{"begin":51,"end":58},"obj":"http://purl.obolibrary.org/obo/GO_0035732"},{"id":"T12","span":{"begin":108,"end":129},"obj":"http://purl.obolibrary.org/obo/GO_0004423"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"GO-CC","denotations":[{"id":"T4","span":{"begin":41,"end":50},"obj":"http://purl.obolibrary.org/obo/GO_0005764"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"EDAM-topics","denotations":[{"id":"T3","span":{"begin":41,"end":50},"obj":"http://edamontology.org/topic_0616"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16377754-3#108#129#gene3423","span":{"begin":108,"end":129},"obj":"gene3423"},{"id":"16377754-3#131#134#gene3423","span":{"begin":131,"end":134},"obj":"gene3423"},{"id":"16377754-3#0#21#diseaseC0026703","span":{"begin":0,"end":21},"obj":"diseaseC0026703"},{"id":"16377754-3#23#26#diseaseC0026703","span":{"begin":23,"end":26},"obj":"diseaseC0026703"},{"id":"16377754-3#0#21#diseaseC0026703","span":{"begin":0,"end":21},"obj":"diseaseC0026703"},{"id":"16377754-3#23#26#diseaseC0026703","span":{"begin":23,"end":26},"obj":"diseaseC0026703"},{"id":"16377754-3#41#67#diseaseC0085078","span":{"begin":41,"end":67},"obj":"diseaseC0085078"}],"relations":[{"id":"108#129#gene34230#21#diseaseC0026703","pred":"associated_with","subj":"16377754-3#108#129#gene3423","obj":"16377754-3#0#21#diseaseC0026703"},{"id":"108#129#gene342323#26#diseaseC0026703","pred":"associated_with","subj":"16377754-3#108#129#gene3423","obj":"16377754-3#23#26#diseaseC0026703"},{"id":"108#129#gene34230#21#diseaseC0026703","pred":"associated_with","subj":"16377754-3#108#129#gene3423","obj":"16377754-3#0#21#diseaseC0026703"},{"id":"108#129#gene342323#26#diseaseC0026703","pred":"associated_with","subj":"16377754-3#108#129#gene3423","obj":"16377754-3#23#26#diseaseC0026703"},{"id":"108#129#gene342341#67#diseaseC0085078","pred":"associated_with","subj":"16377754-3#108#129#gene3423","obj":"16377754-3#41#67#diseaseC0085078"},{"id":"131#134#gene34230#21#diseaseC0026703","pred":"associated_with","subj":"16377754-3#131#134#gene3423","obj":"16377754-3#0#21#diseaseC0026703"},{"id":"131#134#gene342323#26#diseaseC0026703","pred":"associated_with","subj":"16377754-3#131#134#gene3423","obj":"16377754-3#23#26#diseaseC0026703"},{"id":"131#134#gene34230#21#diseaseC0026703","pred":"associated_with","subj":"16377754-3#131#134#gene3423","obj":"16377754-3#0#21#diseaseC0026703"},{"id":"131#134#gene342323#26#diseaseC0026703","pred":"associated_with","subj":"16377754-3#131#134#gene3423","obj":"16377754-3#23#26#diseaseC0026703"},{"id":"131#134#gene342341#67#diseaseC0085078","pred":"associated_with","subj":"16377754-3#131#134#gene3423","obj":"16377754-3#41#67#diseaseC0085078"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":108,"end":129},"obj":"gene:3423"},{"id":"T1","span":{"begin":0,"end":21},"obj":"disease:C0026703"},{"id":"T2","span":{"begin":108,"end":129},"obj":"gene:3423"},{"id":"T3","span":{"begin":23,"end":26},"obj":"disease:C0026703"},{"id":"T4","span":{"begin":108,"end":129},"obj":"gene:3423"},{"id":"T5","span":{"begin":41,"end":67},"obj":"disease:C0085078"},{"id":"T6","span":{"begin":131,"end":134},"obj":"gene:3423"},{"id":"T7","span":{"begin":0,"end":21},"obj":"disease:C0026703"},{"id":"T8","span":{"begin":131,"end":134},"obj":"gene:3423"},{"id":"T9","span":{"begin":23,"end":26},"obj":"disease:C0026703"},{"id":"T10","span":{"begin":131,"end":134},"obj":"gene:3423"},{"id":"T11","span":{"begin":41,"end":67},"obj":"disease:C0085078"}],"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"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}

{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":0,"end":21},"obj":"Disease"},{"id":"T2","span":{"begin":23,"end":26},"obj":"Disease"},{"id":"T3","span":{"begin":41,"end":67},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0019249"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0019249"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"}],"text":"Mucopolysaccharidosis (MPS) type II is a lysosomal storage disorder caused by a deficiency of the exoenzyme iduronate-2-sulfatase (I2S)."}