PubMed:2788166 / 775-1099 JSONTXT

{"project":"Inflammaging","denotations":[{"id":"T5","span":{"begin":0,"end":324},"obj":"Sentence"},{"id":"T5","span":{"begin":0,"end":324},"obj":"Sentence"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T5","span":{"begin":0,"end":324},"obj":"Sentence"},{"id":"T5","span":{"begin":0,"end":324},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"Glycosmos6-MAT","denotations":[{"id":"T5","span":{"begin":248,"end":253},"obj":"http://purl.obolibrary.org/obo/MAT_0000097"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"UBERON-AE","denotations":[{"id":"PD-UBERON-AE-B_T4","span":{"begin":248,"end":253},"obj":"http://purl.obolibrary.org/obo/UBERON_0002107"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"performance-test","denotations":[{"id":"PD-UBERON-AE-B_T4","span":{"begin":248,"end":253},"obj":"http://purl.obolibrary.org/obo/UBERON_0002107"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"HP-phenotype","denotations":[{"id":"T6","span":{"begin":248,"end":261},"obj":"Phenotype"}],"attributes":[{"id":"A6","pred":"hp_id","subj":"T6","obj":"HP:0001392"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"mondo_disease","denotations":[{"id":"T9","span":{"begin":248,"end":261},"obj":"Disease"}],"attributes":[{"id":"A9","pred":"mondo_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/MONDO_0005154"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"Anatomy-UBERON","denotations":[{"id":"T5","span":{"begin":248,"end":253},"obj":"Body_part"}],"attributes":[{"id":"A5","pred":"uberon_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/UBERON_0002107"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}

{"project":"Anatomy-MAT","denotations":[{"id":"T5","span":{"begin":248,"end":253},"obj":"Body_part"}],"attributes":[{"id":"A5","pred":"mat_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/MAT_0000097"}],"text":"Capitalizing on the identification of the homozygous inheritance of the rare Mmalton alpha 1AT deficiency allele, it was demonstrated that although caused by a very different mutation, the Mmalton allele shares with the Z allele the association of liver disease with the same type of abnormalities of alpha 1AT biosynthesis."}