PubMed:16037488 / 0-229 JSONTXT

{"project":"Glycan-Motif","denotations":[{"id":"T1","span":{"begin":150,"end":159},"obj":"https://glytoucan.org/Structures/Glycans/G65889KE"},{"id":"T2","span":{"begin":150,"end":159},"obj":"https://glytoucan.org/Structures/Glycans/G68158BT"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"GlyCosmos6-Glycan-Motif-Image","denotations":[{"id":"T1","span":{"begin":150,"end":159},"obj":"Glycan_Motif"}],"attributes":[{"id":"A1","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G68158BT"},{"id":"A2","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G65889KE"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"GlyCosmos6-Glycan-Motif-Structure","denotations":[{"id":"T1","span":{"begin":150,"end":159},"obj":"https://glytoucan.org/Structures/Glycans/G65889KE"},{"id":"T2","span":{"begin":150,"end":159},"obj":"https://glytoucan.org/Structures/Glycans/G68158BT"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"uniprot-human","denotations":[{"id":"T1","span":{"begin":69,"end":80},"obj":"http://www.uniprot.org/uniprot/P02787"},{"id":"T4","span":{"begin":191,"end":195},"obj":"http://www.uniprot.org/uniprot/Q53XK1"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"uniprot-mouse","denotations":[{"id":"T1","span":{"begin":69,"end":80},"obj":"http://www.uniprot.org/uniprot/Q63915"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"GO-BP","denotations":[{"id":"T1","span":{"begin":33,"end":45},"obj":"http://purl.obolibrary.org/obo/GO_0036065"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"UBERON-AE","denotations":[{"id":"T1","span":{"begin":63,"end":68},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16037488-1#10#30#diseaseC0268151","span":{"begin":128,"end":148},"obj":"diseaseC0268151"},{"id":"16037488-1#73#89#diseaseC0268151","span":{"begin":191,"end":207},"obj":"diseaseC0268151"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":117},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":117},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":117},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"GlycoBiology-Motifs","denotations":[{"id":"T1","span":{"begin":81,"end":90},"obj":"http://rdf.glycoinfo.org/glycan/G00027MO"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"performance-test","denotations":[{"id":"PD-UBERON-AE-B_T1","span":{"begin":63,"end":68},"obj":"http://purl.obolibrary.org/obo/UBERON_0001977"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"DisGeNET","denotations":[{"id":"T1","span":{"begin":128,"end":148},"obj":"disease:C0268151"},{"id":"T3","span":{"begin":191,"end":207},"obj":"disease:C0268151"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":104,"end":116},"obj":"Phenotype"},{"id":"T2","span":{"begin":136,"end":148},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0012024"},{"id":"A2","pred":"hp_id","subj":"T2","obj":"HP:0012024"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":104,"end":116},"obj":"Disease"},{"id":"T3","span":{"begin":128,"end":148},"obj":"Disease"},{"id":"T4","span":{"begin":191,"end":207},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0009258"},{"id":"A2","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0018116"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MONDO_0009258"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/MONDO_0009258"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}

{"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":191,"end":195},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/UBERON_0001962"}],"text":"Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.\nUntreated classic galactosemia (galactose-1-phosphate uridyltransferase [GALT] deficiency) is known as a second"}