PubMed:2788166 / 273-566 JSONTXT

{"project":"Inflammaging","denotations":[{"id":"T3","span":{"begin":0,"end":293},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":293},"obj":"Sentence"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":293},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":293},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"Glycosmos6-MAT","denotations":[{"id":"T4","span":{"begin":279,"end":284},"obj":"http://purl.obolibrary.org/obo/MAT_0000097"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"PubmedHPO","denotations":[{"id":"T2","span":{"begin":48,"end":57},"obj":"HP_0002097"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"UBERON-AE","denotations":[{"id":"PD-UBERON-AE-B_T3","span":{"begin":279,"end":284},"obj":"http://purl.obolibrary.org/obo/UBERON_0002107"},{"id":"PD-UBERON-AE-B_T9","span":{"begin":230,"end":235},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"PubCasesHPO","denotations":[{"id":"AB2","span":{"begin":48,"end":57},"obj":"HP:0002097"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"performance-test","denotations":[{"id":"PD-UBERON-AE-B_T3","span":{"begin":279,"end":284},"obj":"http://purl.obolibrary.org/obo/UBERON_0002107"},{"id":"PD-UBERON-AE-B_T9","span":{"begin":230,"end":235},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"HP-phenotype","denotations":[{"id":"T4","span":{"begin":48,"end":57},"obj":"Phenotype"},{"id":"T5","span":{"begin":279,"end":292},"obj":"Phenotype"}],"attributes":[{"id":"A4","pred":"hp_id","subj":"T4","obj":"HP:0002097"},{"id":"A5","pred":"hp_id","subj":"T5","obj":"HP:0001392"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"mondo_disease","denotations":[{"id":"T5","span":{"begin":48,"end":57},"obj":"Disease"},{"id":"T6","span":{"begin":129,"end":144},"obj":"Disease"},{"id":"T7","span":{"begin":279,"end":292},"obj":"Disease"}],"attributes":[{"id":"A5","pred":"mondo_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MONDO_0004849"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0005154"},{"id":"A7","pred":"mondo_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/MONDO_0005154"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"Anatomy-UBERON","denotations":[{"id":"T4","span":{"begin":279,"end":284},"obj":"Body_part"}],"attributes":[{"id":"A4","pred":"uberon_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/UBERON_0002107"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}

{"project":"Anatomy-MAT","denotations":[{"id":"T4","span":{"begin":279,"end":284},"obj":"Body_part"}],"attributes":[{"id":"A4","pred":"mat_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MAT_0000097"}],"text":"However, whereas there is an increased risk for emphysema associated with at least 10 alpha 1AT deficiency and null alleles, the hepatic disease is observed only in a subset of these alleles, suggesting that it is not the reduced serum levels of alpha 1AT per se which cause the liver disease."}