PubMed:10419498 / 0-241 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/10419498","sourcedb":"PubMed","sourceid":"10419498","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/10419498","text":"Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion.\nMutations in the genes that code for collagen VI subunits, COL6A1, COL6A2, and COL6A3, are the cause of the a","tracks":[{"project":"DisGeNET5_gene_disease","denotations":[{"id":"10419498-1#79#85#gene1293","span":{"begin":211,"end":217},"obj":"gene1293"}],"attributes":[{"subj":"10419498-1#79#85#gene1293","pred":"source","obj":"DisGeNET5_gene_disease"}]},{"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":8,"end":16},"obj":"HP:0003198"}],"attributes":[{"subj":"TI1","pred":"source","obj":"PubCasesHPO"}]},{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":0,"end":16},"obj":"ORDO:610"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"TI1","pred":"source","obj":"PubCasesORDO"}]},{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":131},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":131},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T1","pred":"source","obj":"sentences"},{"subj":"T1","pred":"source","obj":"sentences"}]},{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":8,"end":16},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0003198"},{"subj":"T1","pred":"source","obj":"HP-phenotype"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}]},{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":0,"end":16},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0008029"},{"id":"A2","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0024530"},{"subj":"T1","pred":"source","obj":"mondo_disease"}]},{"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":77,"end":90},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/GO_0005622"},{"subj":"T1","pred":"source","obj":"Anatomy-UBERON"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"DisGeNET5_gene_disease","color":"#93ecb6","default":true},{"id":"PubCasesHPO","color":"#ec9c93"},{"id":"PubCasesORDO","color":"#93a4ec"},{"id":"sentences","color":"#beec93"},{"id":"HP-phenotype","color":"#ec93d8"},{"id":"mondo_disease","color":"#93ece6"},{"id":"Anatomy-UBERON","color":"#eccc93"}]}]}}