PubMed:1794038 / 333-654 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T3","span":{"begin":0,"end":321},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":321},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":321},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"ICD10","denotations":[{"id":"T1","span":{"begin":56,"end":67},"obj":"http://purl.bioontology.org/ontology/ICD10/H10"},{"id":"T2","span":{"begin":56,"end":67},"obj":"http://purl.bioontology.org/ontology/ICD10/H10.9"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"GlycoBiology-FMA","denotations":[{"id":"_T5","span":{"begin":250,"end":262},"obj":"FMAID:196792"},{"id":"_T6","span":{"begin":250,"end":262},"obj":"FMAID:82797"},{"id":"_T7","span":{"begin":264,"end":274},"obj":"FMAID:82750"},{"id":"_T8","span":{"begin":264,"end":274},"obj":"FMAID:196739"}],"namespaces":[{"prefix":"FMAID","uri":"http://purl.org/sig/ont/fma/fma"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"uniprot-human","denotations":[{"id":"T1","span":{"begin":195,"end":197},"obj":"http://www.uniprot.org/uniprot/Q9UCA1"},{"id":"T4","span":{"begin":195,"end":197},"obj":"http://www.uniprot.org/uniprot/Q9UNY4"},{"id":"T7","span":{"begin":202,"end":204},"obj":"http://www.uniprot.org/uniprot/P13726"},{"id":"T10","span":{"begin":284,"end":290},"obj":"http://www.uniprot.org/uniprot/Q96IV0"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"uniprot-mouse","denotations":[{"id":"T1","span":{"begin":195,"end":197},"obj":"http://www.uniprot.org/uniprot/P19221"},{"id":"T4","span":{"begin":202,"end":204},"obj":"http://www.uniprot.org/uniprot/P20352"},{"id":"T7","span":{"begin":284,"end":290},"obj":"http://www.uniprot.org/uniprot/Q9JI78"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"GlycoBiology-NCBITAXON","denotations":[{"id":"T27","span":{"begin":243,"end":247},"obj":"http://purl.bioontology.org/ontology/NCBITAXON/3554"},{"id":"T28","span":{"begin":243,"end":247},"obj":"http://purl.bioontology.org/ontology/NCBITAXON/158455"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"GO-BP","denotations":[{"id":"T1","span":{"begin":93,"end":101},"obj":"http://purl.obolibrary.org/obo/GO_0015297"},{"id":"T2","span":{"begin":284,"end":290},"obj":"http://purl.obolibrary.org/obo/GO_0000224"},{"id":"T4","span":{"begin":284,"end":292},"obj":"http://purl.obolibrary.org/obo/GO_0000224"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"EDAM-topics","denotations":[{"id":"T1","span":{"begin":26,"end":37},"obj":"http://edamontology.org/topic_0602"},{"id":"T2","span":{"begin":223,"end":230},"obj":"http://edamontology.org/topic_0154"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"EDAM-DFO","denotations":[{"id":"T3","span":{"begin":223,"end":230},"obj":"http://edamontology.org/data_2906"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"NGLY1-deficiency","denotations":[{"id":"PD-NGLY1-deficiency-B_T1","span":{"begin":234,"end":262},"obj":"chem:24139"},{"id":"PD-NGLY1-deficiency-B_T2","span":{"begin":284,"end":290},"obj":"hgnc:17646"}],"namespaces":[{"prefix":"hgnc","uri":"https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:"},{"prefix":"omim","uri":"https://www.omim.org/entry/"},{"prefix":"chem","uri":"https://pubchem.ncbi.nlm.nih.gov/compound/"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}

{"project":"GlycoBiology-Epitope","denotations":[{"id":"PD-GlycoEpitope-B_T2","span":{"begin":191,"end":193},"obj":"http://www.glycoepitope.jp/epitopes/AN0591"}],"text":"FPLC-directed hydrophobic-interaction chromatography in conjunction with high-resolution ion-exchange chromatography provided a more simple, rapid method for the isolation of endoglycosidase F1, F2 and F3, and the amidase, peptide-N4-N-acetyl-beta-D-glucosaminyl)-asparagine amidase (PNGase F), in greater than 50% yield."}