PubMed:23514716 / 872-1150
Annnotations
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T9","span":{"begin":0,"end":278},"obj":"Sentence"},{"id":"T8","span":{"begin":0,"end":278},"obj":"Sentence"},{"id":"T9","span":{"begin":0,"end":278},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlycoBiology-GDGDB
{"project":"GlycoBiology-GDGDB","denotations":[{"id":"_T1","span":{"begin":162,"end":189},"obj":"http://acgg.asia/db/diseases/gdgdb?con_ui=CON00384"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
ICD10
{"project":"ICD10","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"http://purl.bioontology.org/ontology/ICD10/G71.0"},{"id":"T2","span":{"begin":171,"end":189},"obj":"http://purl.bioontology.org/ontology/ICD10/G71.0"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlycoBiology-FMA
{"project":"GlycoBiology-FMA","denotations":[{"id":"_T36","span":{"begin":127,"end":139},"obj":"FMAID:62357"},{"id":"_T37","span":{"begin":127,"end":139},"obj":"FMAID:165876"},{"id":"_T38","span":{"begin":180,"end":189},"obj":"FMAID:165876"},{"id":"_T39","span":{"begin":180,"end":189},"obj":"FMAID:62357"},{"id":"_T40","span":{"begin":275,"end":277},"obj":"FMAID:177171"}],"namespaces":[{"prefix":"FMAID","uri":"http://purl.org/sig/ont/fma/fma"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
uniprot-mouse
{"project":"uniprot-mouse","denotations":[{"id":"T7","span":{"begin":52,"end":56},"obj":"http://www.uniprot.org/uniprot/Q61419"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlycoBiology-NCBITAXON
{"project":"GlycoBiology-NCBITAXON","denotations":[{"id":"T6","span":{"begin":107,"end":114},"obj":"http://purl.bioontology.org/ontology/NCBITAXON/353209"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
EDAM-DFO
{"project":"EDAM-DFO","denotations":[{"id":"T1","span":{"begin":12,"end":24},"obj":"http://edamontology.org/operation_2246"},{"id":"T2","span":{"begin":98,"end":106},"obj":"http://edamontology.org/data_3108"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
PubmedHPO
{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"HP_0003560"},{"id":"T2","span":{"begin":171,"end":189},"obj":"HP_0003560"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
mondo_disease
{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"Disease"},{"id":"T2","span":{"begin":162,"end":189},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0020121"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0010679"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlyCosmos15-HP
{"project":"GlyCosmos15-HP","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"Phenotype"},{"id":"T2","span":{"begin":171,"end":189},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0003560"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0003560"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlyCosmos15-MONDO
{"project":"GlyCosmos15-MONDO","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"Disease"},{"id":"T2","span":{"begin":162,"end":189},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0020121"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0010679"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlyCosmos15-NCBITAXON
{"project":"GlyCosmos15-NCBITAXON","denotations":[{"id":"T8","span":{"begin":46,"end":51},"obj":"OrganismTaxon"},{"id":"T10","span":{"begin":144,"end":148},"obj":"OrganismTaxon"}],"attributes":[{"id":"A8","pred":"db_id","subj":"T8","obj":"10088"},{"id":"A9","pred":"db_id","subj":"T8","obj":"10090"},{"id":"A10","pred":"db_id","subj":"T10","obj":"10088"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T9","span":{"begin":0,"end":278},"obj":"Sentence"},{"id":"T8","span":{"begin":0,"end":278},"obj":"Sentence"},{"id":"T9","span":{"begin":0,"end":278},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
GlyCosmos15-Sentences
{"project":"GlyCosmos15-Sentences","blocks":[{"id":"T8","span":{"begin":0,"end":278},"obj":"Sentence"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
NCBITAXON
{"project":"NCBITAXON","denotations":[{"id":"T8","span":{"begin":46,"end":51},"obj":"OrganismTaxon"},{"id":"T10","span":{"begin":144,"end":148},"obj":"OrganismTaxon"}],"attributes":[{"id":"A8","pred":"db_id","subj":"T8","obj":"10088"},{"id":"A9","pred":"db_id","subj":"T8","obj":"10090"},{"id":"A10","pred":"db_id","subj":"T10","obj":"10088"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}
HP-phenotype
{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":118,"end":136},"obj":"Phenotype"},{"id":"T2","span":{"begin":171,"end":189},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0003560"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0003560"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"We recently demonstrated that the deletion of mouse Cmah worsened the severity of pathophysiology measures related to muscular dystrophy in mdx mice, a model for Duchenne muscular dystrophy (Chandrasekharan K, Yoon JH, Xu Y, deVries S, Camboni M, Janssen PM, Varki A, Martin PT."}