CORD-19:85fe4d02c970252bd374d09ceb879165c7f6e8f6 / 18142-18636 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"TextSentencer_T107","span":{"begin":0,"end":494},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Although this is an attractive model, 738 the fact that a deletion encompassing the high affinity hnRNP A1 binding site in the 3'UTR is 739 able to replicate and direct normal synthesis of subgenomic mRNAs makes the PTB-hnRNP A1 740 association less likely to have a crucial role in leader-body rejoining (Goebel et al., 2007) , 741 although the possibility that other members of the hnRNP family could substitute for hnRNP A1 742 remains a possibility (see section 5 for a discussion of this)."}

{"project":"Epistemic_Statements","denotations":[{"id":"T50","span":{"begin":0,"end":494},"obj":"Epistemic_statement"}],"text":"Although this is an attractive model, 738 the fact that a deletion encompassing the high affinity hnRNP A1 binding site in the 3'UTR is 739 able to replicate and direct normal synthesis of subgenomic mRNAs makes the PTB-hnRNP A1 740 association less likely to have a crucial role in leader-body rejoining (Goebel et al., 2007) , 741 although the possibility that other members of the hnRNP family could substitute for hnRNP A1 742 remains a possibility (see section 5 for a discussion of this)."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T107","span":{"begin":0,"end":494},"obj":"Sentence"}],"text":"Although this is an attractive model, 738 the fact that a deletion encompassing the high affinity hnRNP A1 binding site in the 3'UTR is 739 able to replicate and direct normal synthesis of subgenomic mRNAs makes the PTB-hnRNP A1 740 association less likely to have a crucial role in leader-body rejoining (Goebel et al., 2007) , 741 although the possibility that other members of the hnRNP family could substitute for hnRNP A1 742 remains a possibility (see section 5 for a discussion of this)."}