PubMed:23528641 / 0-157 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":131},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":131},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"263.4 kb deletion within the TCF4 gene consistent with Pitt-Hopkins syndrome, inherited from a mosaic parent with normal phenotype.\nPitt-Hopkins syndrome (PT"}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":29,"end":33},"obj":"gene:6934"},{"id":"T1","span":{"begin":55,"end":76},"obj":"disease:C1970431"},{"id":"T2","span":{"begin":29,"end":33},"obj":"gene:6925"},{"id":"T3","span":{"begin":55,"end":76},"obj":"disease:C1970431"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"},{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"263.4 kb deletion within the TCF4 gene consistent with Pitt-Hopkins syndrome, inherited from a mosaic parent with normal phenotype.\nPitt-Hopkins syndrome (PT"}

{"project":"Allie","denotations":[{"id":"SS1_23528641_1_0","span":{"begin":132,"end":153},"obj":"expanded"}],"text":"263.4 kb deletion within the TCF4 gene consistent with Pitt-Hopkins syndrome, inherited from a mosaic parent with normal phenotype.\nPitt-Hopkins syndrome (PT"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"23528641-0#29#33#gene6925","span":{"begin":29,"end":33},"obj":"gene6925"},{"id":"23528641-0#55#76#diseaseC1970431","span":{"begin":55,"end":76},"obj":"diseaseC1970431"}],"relations":[{"id":"29#33#gene692555#76#diseaseC1970431","pred":"associated_with","subj":"23528641-0#29#33#gene6925","obj":"23528641-0#55#76#diseaseC1970431"}],"text":"263.4 kb deletion within the TCF4 gene consistent with Pitt-Hopkins syndrome, inherited from a mosaic parent with normal phenotype.\nPitt-Hopkins syndrome (PT"}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":132,"end":153},"obj":"ORDO:2896"},{"id":"TI1","span":{"begin":55,"end":76},"obj":"ORDO:2896"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"263.4 kb deletion within the TCF4 gene consistent with Pitt-Hopkins syndrome, inherited from a mosaic parent with normal phenotype.\nPitt-Hopkins syndrome (PT"}