PubMed:21497194 / 0-298 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":97},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":97},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":159,"end":177},"obj":"gene:2720"},{"id":"T1","span":{"begin":121,"end":139},"obj":"disease:C0086652"},{"id":"T2","span":{"begin":159,"end":177},"obj":"gene:2720"},{"id":"T3","span":{"begin":179,"end":195},"obj":"disease:C0268271"},{"id":"T4","span":{"begin":159,"end":177},"obj":"gene:2720"},{"id":"T5","span":{"begin":179,"end":195},"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":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"21497194-1#61#79#gene2720","span":{"begin":159,"end":177},"obj":"gene2720"},{"id":"21497194-1#81#97#diseaseC2718068","span":{"begin":179,"end":195},"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":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":98,"end":116},"obj":"ORDO:354"},{"id":"AB2","span":{"begin":179,"end":195},"obj":"ORDO:354"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":0,"end":18},"obj":"Disease"},{"id":"T2","span":{"begin":98,"end":116},"obj":"Disease"},{"id":"T3","span":{"begin":178,"end":195},"obj":"Disease"},{"id":"T4","span":{"begin":211,"end":237},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0018149"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0018149"},{"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":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"Glycan-GlyCosmos","denotations":[{"id":"T1","span":{"begin":0,"end":3},"obj":"Glycan"},{"id":"T2","span":{"begin":98,"end":101},"obj":"Glycan"}],"attributes":[{"id":"A1","pred":"glycosmos_id","subj":"T1","obj":"https://glycosmos.org/glycans/show/G48558GR"},{"id":"A8","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR"},{"id":"A2","pred":"glycosmos_id","subj":"T2","obj":"https://glycosmos.org/glycans/show/G48558GR"},{"id":"A9","pred":"image","subj":"T2","obj":"https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"GlyCosmos-GlycoEpitope","denotations":[{"id":"T1","span":{"begin":0,"end":3},"obj":"http://purl.jp/bio/12/glyco/glycan#Glycan_epitope"},{"id":"T2","span":{"begin":98,"end":101},"obj":"http://purl.jp/bio/12/glyco/glycan#Glycan_epitope"}],"attributes":[{"id":"A1","pred":"glycoepitope_id","subj":"T1","obj":"http://www.glycoepitope.jp/epitopes/EP0050"},{"id":"A2","pred":"glycoepitope_id","subj":"T2","obj":"http://www.glycoepitope.jp/epitopes/EP0050"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"GlyCosmos15-MONDO","denotations":[{"id":"T1","span":{"begin":0,"end":18},"obj":"Disease"},{"id":"T2","span":{"begin":98,"end":116},"obj":"Disease"},{"id":"T3","span":{"begin":178,"end":195},"obj":"Disease"},{"id":"T4","span":{"begin":211,"end":237},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0018149"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0018149"},{"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":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":97},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":97},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"GlyCosmos15-Sentences","blocks":[{"id":"T1","span":{"begin":0,"end":97},"obj":"Sentence"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"GlyCosmos15-Glycan","denotations":[{"id":"T1","span":{"begin":0,"end":3},"obj":"Glycan"},{"id":"T2","span":{"begin":98,"end":101},"obj":"Glycan"}],"attributes":[{"id":"A1","pred":"glycosmos_id","subj":"T1","obj":"https://glycosmos.org/glycans/show/G48558GR"},{"id":"A8","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR"},{"id":"A2","pred":"glycosmos_id","subj":"T2","obj":"https://glycosmos.org/glycans/show/G48558GR"},{"id":"A9","pred":"image","subj":"T2","obj":"https://api.glycosmos.org/wurcs2image/latest/png/binary/G48558GR"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}

{"project":"GlyCosmos15-GlycoEpitope","denotations":[{"id":"T1","span":{"begin":0,"end":3},"obj":"http://purl.jp/bio/12/glyco/glycan#Glycan_epitope"},{"id":"T2","span":{"begin":98,"end":101},"obj":"http://purl.jp/bio/12/glyco/glycan#Glycan_epitope"}],"attributes":[{"id":"A1","pred":"glycoepitope_id","subj":"T1","obj":"http://www.glycoepitope.jp/epitopes/EP0050"},{"id":"A2","pred":"glycoepitope_id","subj":"T2","obj":"http://www.glycoepitope.jp/epitopes/EP0050"}],"text":"GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings.\nGM1 gangliosidosis 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 w"}