PubMed:16423994 / 1321-1625 JSONTXT

{"project":"c_corpus","denotations":[{"id":"T217","span":{"begin":29,"end":34},"obj":"CHEBI:50406"},{"id":"T216","span":{"begin":29,"end":34},"obj":"SO:0000051"},{"id":"T218","span":{"begin":128,"end":132},"obj":"PR:Q9ZRV4"},{"id":"T219","span":{"begin":128,"end":132},"obj":"PR:P38920"},{"id":"T220","span":{"begin":128,"end":132},"obj":"PR:Q54KD8"},{"id":"T222","span":{"begin":128,"end":132},"obj":"PR:Q9JK91"},{"id":"T223","span":{"begin":128,"end":132},"obj":"PR:P97679"},{"id":"T224","span":{"begin":128,"end":132},"obj":"PR:Q9P7W6"},{"id":"T225","span":{"begin":128,"end":132},"obj":"PR:000010442"},{"id":"T226","span":{"begin":128,"end":132},"obj":"PR:P40692"},{"id":"T221","span":{"begin":128,"end":132},"obj":"CVCL_G669"},{"id":"T228","span":{"begin":133,"end":136},"obj":"CHEBI:16768"},{"id":"T232","span":{"begin":133,"end":136},"obj":"D009074"},{"id":"T233","span":{"begin":133,"end":136},"obj":"D009074"},{"id":"T234","span":{"begin":133,"end":137},"obj":"PR:000010666"},{"id":"T235","span":{"begin":133,"end":137},"obj":"PR:P25847"},{"id":"T236","span":{"begin":133,"end":137},"obj":"PR:P43246"},{"id":"T237","span":{"begin":133,"end":137},"obj":"P22711"},{"id":"T238","span":{"begin":133,"end":137},"obj":"PR:P22711"},{"id":"T239","span":{"begin":133,"end":137},"obj":"PR:P54275"},{"id":"T240","span":{"begin":133,"end":137},"obj":"PR:O74773"},{"id":"T241","span":{"begin":133,"end":137},"obj":"PR:P43247"},{"id":"T242","span":{"begin":133,"end":137},"obj":"PR:Q553L4"},{"id":"T243","span":{"begin":133,"end":137},"obj":"PR:O24617"},{"id":"T244","span":{"begin":138,"end":146},"obj":"SO:0000159"},{"id":"T245","span":{"begin":147,"end":155},"obj":"CHEBI:78059"},{"id":"T246","span":{"begin":247,"end":265},"obj":"D015179"},{"id":"T247","span":{"begin":247,"end":265},"obj":"D015179"}],"text":"Multiplex ligation-dependent probe amplification analysis of 18 cancer specimens from two independent sets of Swiss and Finnish MLH1/MSH2 deletion carriers revealed that somatic mutations identical to the ones in the germ line occur frequently in colorectal cancers (6 of 11; 55%) and are also present in"}

{"project":"PubmedHPO","denotations":[{"id":"T8","span":{"begin":64,"end":70},"obj":"HP_0002664"},{"id":"T9","span":{"begin":170,"end":187},"obj":"HP_0001428"},{"id":"T10","span":{"begin":258,"end":265},"obj":"HP_0002664"}],"text":"Multiplex ligation-dependent probe amplification analysis of 18 cancer specimens from two independent sets of Swiss and Finnish MLH1/MSH2 deletion carriers revealed that somatic mutations identical to the ones in the germ line occur frequently in colorectal cancers (6 of 11; 55%) and are also present in"}

{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T7","span":{"begin":0,"end":304},"obj":"DRI_Background"}],"text":"Multiplex ligation-dependent probe amplification analysis of 18 cancer specimens from two independent sets of Swiss and Finnish MLH1/MSH2 deletion carriers revealed that somatic mutations identical to the ones in the germ line occur frequently in colorectal cancers (6 of 11; 55%) and are also present in"}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16423994-6#128#132#gene4292","span":{"begin":128,"end":132},"obj":"gene4292"},{"id":"16423994-6#133#137#gene4436","span":{"begin":133,"end":137},"obj":"gene4436"},{"id":"16423994-6#247#265#diseaseC1527249","span":{"begin":247,"end":265},"obj":"diseaseC1527249"},{"id":"16423994-6#247#265#diseaseC1527249","span":{"begin":247,"end":265},"obj":"diseaseC1527249"}],"relations":[{"id":"128#132#gene4292247#265#diseaseC1527249","pred":"associated_with","subj":"16423994-6#128#132#gene4292","obj":"16423994-6#247#265#diseaseC1527249"},{"id":"128#132#gene4292247#265#diseaseC1527249","pred":"associated_with","subj":"16423994-6#128#132#gene4292","obj":"16423994-6#247#265#diseaseC1527249"},{"id":"133#137#gene4436247#265#diseaseC1527249","pred":"associated_with","subj":"16423994-6#133#137#gene4436","obj":"16423994-6#247#265#diseaseC1527249"},{"id":"133#137#gene4436247#265#diseaseC1527249","pred":"associated_with","subj":"16423994-6#133#137#gene4436","obj":"16423994-6#247#265#diseaseC1527249"}],"text":"Multiplex ligation-dependent probe amplification analysis of 18 cancer specimens from two independent sets of Swiss and Finnish MLH1/MSH2 deletion carriers revealed that somatic mutations identical to the ones in the germ line occur frequently in colorectal cancers (6 of 11; 55%) and are also present in"}

{"project":"DisGeNET","denotations":[{"id":"T6","span":{"begin":133,"end":137},"obj":"gene:4436"},{"id":"T8","span":{"begin":133,"end":137},"obj":"gene:4436"},{"id":"T9","span":{"begin":247,"end":265},"obj":"disease:C1527249"},{"id":"T10","span":{"begin":128,"end":132},"obj":"gene:4292"},{"id":"T12","span":{"begin":128,"end":132},"obj":"gene:4292"},{"id":"T13","span":{"begin":247,"end":265},"obj":"disease:C1527249"}],"relations":[{"id":"R5","pred":"associated_with","subj":"T8","obj":"T9"},{"id":"R7","pred":"associated_with","subj":"T12","obj":"T13"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Multiplex ligation-dependent probe amplification analysis of 18 cancer specimens from two independent sets of Swiss and Finnish MLH1/MSH2 deletion carriers revealed that somatic mutations identical to the ones in the germ line occur frequently in colorectal cancers (6 of 11; 55%) and are also present in"}