PubMed:2788166 / 0-207 JSONTXT

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{"project":"Anatomy-MAT","denotations":[{"id":"T1","span":{"begin":23,"end":28},"obj":"Body_part"},{"id":"T2","span":{"begin":33,"end":37},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"mat_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MAT_0000097"},{"id":"A2","pred":"mat_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MAT_0000135"}],"text":"Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency allele Mmalton.\nAlpha 1-Antitrypsin (alpha 1AT) deficiency is characterized by reduced serum levels of alpha 1"}