CORD-19:02d18b4f484a0420c21595a95b8765125d4a484c / 41218-41381 JSONTXT

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T233","span":{"begin":0,"end":163},"obj":"Sentence"}],"text":"Gene mutations in the B 0 AT1 (Slc6a19) neutral amino acid transporter were identified as one cause of Hartnup's disorder (Kleta et al., 2004; Seow et al., 2004) ."}

{"project":"CORD-19-Sentences","denotations":[{"id":"TextSentencer_T233","span":{"begin":0,"end":163},"obj":"Sentence"},{"id":"TextSentencer_T233","span":{"begin":0,"end":163},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Gene mutations in the B 0 AT1 (Slc6a19) neutral amino acid transporter were identified as one cause of Hartnup's disorder (Kleta et al., 2004; Seow et al., 2004) ."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T268","span":{"begin":26,"end":29},"obj":"Disease"},{"id":"T269","span":{"begin":103,"end":121},"obj":"Disease"}],"attributes":[{"id":"A268","pred":"mondo_id","subj":"T268","obj":"http://purl.obolibrary.org/obo/MONDO_0008840"},{"id":"A269","pred":"mondo_id","subj":"T269","obj":"http://purl.obolibrary.org/obo/MONDO_0009324"}],"text":"Gene mutations in the B 0 AT1 (Slc6a19) neutral amino acid transporter were identified as one cause of Hartnup's disorder (Kleta et al., 2004; Seow et al., 2004) ."}