PubMed:25533456 / 503-688 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T4","span":{"begin":0,"end":185},"obj":"Sentence"},{"id":"T4","span":{"begin":0,"end":185},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}

    PubmedHPO

    {"project":"PubmedHPO","denotations":[{"id":"T5","span":{"begin":107,"end":115},"obj":"HP_0003198"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}

    PubCasesHPO

    {"project":"PubCasesHPO","denotations":[{"id":"AB4","span":{"begin":109,"end":117},"obj":"HP:0003198"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"AB3","span":{"begin":99,"end":115},"obj":"ORDO:610"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}

    HP-phenotype

    {"project":"HP-phenotype","denotations":[{"id":"T5","span":{"begin":107,"end":115},"obj":"Phenotype"}],"attributes":[{"id":"A5","pred":"hp_id","subj":"T5","obj":"HP:0003198"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T11","span":{"begin":99,"end":115},"obj":"Disease"}],"attributes":[{"id":"A11","pred":"mondo_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/MONDO_0008029"},{"id":"A12","pred":"mondo_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/MONDO_0024530"}],"text":"Dominant and recessive mutations are found across the entire clinical spectrum; however, recessive Bethlem myopathy is rare, and our understanding of the molecular pathology is limited."}