PubMed:16423994 / 125-408 JSONTXT

{"project":"c_corpus","denotations":[{"id":"T34","span":{"begin":24,"end":41},"obj":"D015179"},{"id":"T35","span":{"begin":24,"end":41},"obj":"D015179"},{"id":"T36","span":{"begin":151,"end":154},"obj":"GO:0005574"},{"id":"T38","span":{"begin":151,"end":154},"obj":"SO:0000352"},{"id":"T37","span":{"begin":151,"end":154},"obj":"CHEBI:16991"},{"id":"T39","span":{"begin":151,"end":154},"obj":"D004247"},{"id":"T40","span":{"begin":155,"end":170},"obj":"GO:0006298"},{"id":"T41","span":{"begin":192,"end":196},"obj":"PR:Q9ZRV4"},{"id":"T42","span":{"begin":192,"end":196},"obj":"PR:P38920"},{"id":"T43","span":{"begin":192,"end":196},"obj":"PR:Q54KD8"},{"id":"T45","span":{"begin":192,"end":196},"obj":"PR:Q9JK91"},{"id":"T46","span":{"begin":192,"end":196},"obj":"PR:P97679"},{"id":"T47","span":{"begin":192,"end":196},"obj":"PR:Q9P7W6"},{"id":"T48","span":{"begin":192,"end":196},"obj":"PR:000010442"},{"id":"T49","span":{"begin":192,"end":196},"obj":"PR:P40692"},{"id":"T44","span":{"begin":192,"end":196},"obj":"CVCL_G669"},{"id":"T51","span":{"begin":201,"end":204},"obj":"CHEBI:16768"},{"id":"T55","span":{"begin":201,"end":204},"obj":"D009074"},{"id":"T56","span":{"begin":201,"end":204},"obj":"D009074"},{"id":"T57","span":{"begin":201,"end":205},"obj":"PR:000010666"},{"id":"T58","span":{"begin":201,"end":205},"obj":"PR:P25847"},{"id":"T59","span":{"begin":201,"end":205},"obj":"PR:P43246"},{"id":"T60","span":{"begin":201,"end":205},"obj":"P22711"},{"id":"T61","span":{"begin":201,"end":205},"obj":"PR:P22711"},{"id":"T62","span":{"begin":201,"end":205},"obj":"PR:P54275"},{"id":"T63","span":{"begin":201,"end":205},"obj":"PR:O74773"},{"id":"T64","span":{"begin":201,"end":205},"obj":"PR:P43247"},{"id":"T65","span":{"begin":201,"end":205},"obj":"PR:Q553L4"},{"id":"T66","span":{"begin":201,"end":205},"obj":"PR:O24617"}],"text":"Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, predominantly MLH1 and MSH2, with large genomic rearrangements accounting for 5% to 20% of all mutations."}

{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":35,"end":41},"obj":"HP_0002664"},{"id":"T2","span":{"begin":56,"end":76},"obj":"HP_0000006"},{"id":"T3","span":{"begin":56,"end":86},"obj":"HP_0000006"},{"id":"T4","span":{"begin":87,"end":93},"obj":"HP_0002664"}],"text":"Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, predominantly MLH1 and MSH2, with large genomic rearrangements accounting for 5% to 20% of all mutations."}

{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T2","span":{"begin":0,"end":283},"obj":"DRI_Background"}],"text":"Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, predominantly MLH1 and MSH2, with large genomic rearrangements accounting for 5% to 20% of all mutations."}

{"project":"DisGeNET","denotations":[{"id":"T2","span":{"begin":201,"end":205},"obj":"gene:4436"},{"id":"T3","span":{"begin":0,"end":41},"obj":"disease:C1333990"},{"id":"T4","span":{"begin":192,"end":196},"obj":"gene:4292"},{"id":"T5","span":{"begin":0,"end":41},"obj":"disease:C1333990"}],"relations":[{"id":"R2","pred":"associated_with","subj":"T2","obj":"T3"},{"id":"R3","pred":"associated_with","subj":"T4","obj":"T5"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, predominantly MLH1 and MSH2, with large genomic rearrangements accounting for 5% to 20% of all mutations."}