CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 870685-870948 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T3535","span":{"begin":0,"end":263},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A (GGGGCC)n hexanucleotide repeat expansion in an intronic region of the C9orf72 gene has been observed in the general population with a frequency of ~1/600 and is present in ~10% of all amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) cases."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T395","span":{"begin":0,"end":263},"obj":"Sentence"}],"text":"A (GGGGCC)n hexanucleotide repeat expansion in an intronic region of the C9orf72 gene has been observed in the general population with a frequency of ~1/600 and is present in ~10% of all amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) cases."}

{"project":"CORD-19-PD-HP","denotations":[{"id":"T1772","span":{"begin":187,"end":216},"obj":"Phenotype"},{"id":"T1773","span":{"begin":218,"end":221},"obj":"Phenotype"},{"id":"T1774","span":{"begin":227,"end":250},"obj":"Phenotype"},{"id":"T1775","span":{"begin":252,"end":255},"obj":"Phenotype"}],"attributes":[{"id":"A1772","pred":"hp_id","subj":"T1772","obj":"http://purl.obolibrary.org/obo/HP_0007354"},{"id":"A1773","pred":"hp_id","subj":"T1773","obj":"http://purl.obolibrary.org/obo/HP_0007354"},{"id":"A1774","pred":"hp_id","subj":"T1774","obj":"http://purl.obolibrary.org/obo/HP_0002145"},{"id":"A1775","pred":"hp_id","subj":"T1775","obj":"http://purl.obolibrary.org/obo/HP_0002145"}],"text":"A (GGGGCC)n hexanucleotide repeat expansion in an intronic region of the C9orf72 gene has been observed in the general population with a frequency of ~1/600 and is present in ~10% of all amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) cases."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T3800","span":{"begin":187,"end":216},"obj":"Disease"},{"id":"T3801","span":{"begin":199,"end":216},"obj":"Disease"},{"id":"T3802","span":{"begin":218,"end":221},"obj":"Disease"},{"id":"T3803","span":{"begin":227,"end":250},"obj":"Disease"},{"id":"T3805","span":{"begin":242,"end":250},"obj":"Disease"},{"id":"T3806","span":{"begin":252,"end":255},"obj":"Disease"},{"id":"T36730","span":{"begin":187,"end":216},"obj":"Disease"},{"id":"T12989","span":{"begin":199,"end":216},"obj":"Disease"},{"id":"T36051","span":{"begin":218,"end":221},"obj":"Disease"},{"id":"T42711","span":{"begin":227,"end":250},"obj":"Disease"},{"id":"T7464","span":{"begin":242,"end":250},"obj":"Disease"},{"id":"T99897","span":{"begin":252,"end":255},"obj":"Disease"}],"attributes":[{"id":"A3800","pred":"mondo_id","subj":"T3800","obj":"http://purl.obolibrary.org/obo/MONDO_0004976"},{"id":"A3801","pred":"mondo_id","subj":"T3801","obj":"http://purl.obolibrary.org/obo/MONDO_0018155"},{"id":"A3802","pred":"mondo_id","subj":"T3802","obj":"http://purl.obolibrary.org/obo/MONDO_0004976"},{"id":"A3803","pred":"mondo_id","subj":"T3803","obj":"http://purl.obolibrary.org/obo/MONDO_0010857"},{"id":"A3804","pred":"mondo_id","subj":"T3803","obj":"http://purl.obolibrary.org/obo/MONDO_0017276"},{"id":"A3805","pred":"mondo_id","subj":"T3805","obj":"http://purl.obolibrary.org/obo/MONDO_0001627"},{"id":"A3806","pred":"mondo_id","subj":"T3806","obj":"http://purl.obolibrary.org/obo/MONDO_0010857"},{"id":"A3807","pred":"mondo_id","subj":"T3806","obj":"http://purl.obolibrary.org/obo/MONDO_0017276"},{"id":"A52417","pred":"mondo_id","subj":"T36730","obj":"http://purl.obolibrary.org/obo/MONDO_0004976"},{"id":"A13429","pred":"mondo_id","subj":"T12989","obj":"http://purl.obolibrary.org/obo/MONDO_0018155"},{"id":"A61147","pred":"mondo_id","subj":"T36051","obj":"http://purl.obolibrary.org/obo/MONDO_0004976"},{"id":"A79150","pred":"mondo_id","subj":"T42711","obj":"http://purl.obolibrary.org/obo/MONDO_0010857"},{"id":"A62716","pred":"mondo_id","subj":"T42711","obj":"http://purl.obolibrary.org/obo/MONDO_0017276"},{"id":"A80561","pred":"mondo_id","subj":"T7464","obj":"http://purl.obolibrary.org/obo/MONDO_0001627"},{"id":"A87593","pred":"mondo_id","subj":"T99897","obj":"http://purl.obolibrary.org/obo/MONDO_0010857"},{"id":"A61491","pred":"mondo_id","subj":"T99897","obj":"http://purl.obolibrary.org/obo/MONDO_0017276"}],"text":"A (GGGGCC)n hexanucleotide repeat expansion in an intronic region of the C9orf72 gene has been observed in the general population with a frequency of ~1/600 and is present in ~10% of all amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) cases."}