PubMed:21497194 / 116-313 JSONTXT

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":43,"end":61},"obj":"gene:2720"},{"id":"T1","span":{"begin":5,"end":23},"obj":"disease:C0086652"},{"id":"T2","span":{"begin":43,"end":61},"obj":"gene:2720"},{"id":"T3","span":{"begin":63,"end":79},"obj":"disease:C0268271"},{"id":"T4","span":{"begin":43,"end":61},"obj":"gene:2720"},{"id":"T5","span":{"begin":63,"end":79},"obj":"disease:C2718068"}],"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"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"21497194-1#61#79#gene2720","span":{"begin":43,"end":61},"obj":"gene2720"},{"id":"21497194-1#81#97#diseaseC2718068","span":{"begin":63,"end":79},"obj":"diseaseC2718068"}],"relations":[{"id":"61#79#gene272081#97#diseaseC2718068","pred":"associated_with","subj":"21497194-1#61#79#gene2720","obj":"21497194-1#81#97#diseaseC2718068"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}

{"project":"PubCasesORDO","denotations":[{"id":"AB2","span":{"begin":63,"end":79},"obj":"ORDO:354"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}

{"project":"mondo_disease","denotations":[{"id":"T3","span":{"begin":62,"end":79},"obj":"Disease"},{"id":"T4","span":{"begin":95,"end":121},"obj":"Disease"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0018149"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}

{"project":"GlyCosmos15-MONDO","denotations":[{"id":"T3","span":{"begin":15,"end":23},"obj":"Disease"},{"id":"T4","span":{"begin":62,"end":79},"obj":"Disease"},{"id":"T5","span":{"begin":95,"end":121},"obj":"Disease"}],"attributes":[{"id":"A3","pred":"mondo_id","subj":"T3","obj":"MONDO:0002254"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"MONDO:0018149"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"MONDO:0002561"}],"namespaces":[{"prefix":"MONDO","uri":"http://purl.obolibrary.org/obo/MONDO_"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}

{"project":"GlyCosmos15-FMA","denotations":[{"id":"T1","span":{"begin":95,"end":104},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"FMA:63836"}],"namespaces":[{"prefix":"FMA","uri":"http://purl.org/sig/ont/fma/fma"}],"text":" and Morquio B syndrome, both arising from beta-galactosidase (GLB1) deficiency, are very rare lysosomal storage diseases with an incidence of about 1:100,000-1:200,000 live births worldwide. Here "}