PubMed:16423994 / 0-304
Annnotations
c_corpus
{"project":"c_corpus","denotations":[{"id":"T1","span":{"begin":0,"end":15},"obj":"GO:0035822"},{"id":"T2","span":{"begin":63,"end":72},"obj":"SO:0000817"},{"id":"T3","span":{"begin":73,"end":79},"obj":"SO:0001023"},{"id":"T4","span":{"begin":83,"end":90},"obj":"D009369"},{"id":"T5","span":{"begin":83,"end":90},"obj":"D009369"},{"id":"T6","span":{"begin":96,"end":100},"obj":"PR:Q9ZRV4"},{"id":"T7","span":{"begin":96,"end":100},"obj":"PR:P38920"},{"id":"T8","span":{"begin":96,"end":100},"obj":"PR:Q54KD8"},{"id":"T10","span":{"begin":96,"end":100},"obj":"PR:Q9JK91"},{"id":"T11","span":{"begin":96,"end":100},"obj":"PR:P97679"},{"id":"T12","span":{"begin":96,"end":100},"obj":"PR:Q9P7W6"},{"id":"T13","span":{"begin":96,"end":100},"obj":"PR:000010442"},{"id":"T14","span":{"begin":96,"end":100},"obj":"PR:P40692"},{"id":"T9","span":{"begin":96,"end":100},"obj":"CVCL_G669"},{"id":"T16","span":{"begin":101,"end":104},"obj":"CHEBI:16768"},{"id":"T20","span":{"begin":101,"end":104},"obj":"D009074"},{"id":"T21","span":{"begin":101,"end":104},"obj":"D009074"},{"id":"T22","span":{"begin":101,"end":105},"obj":"PR:000010666"},{"id":"T23","span":{"begin":101,"end":105},"obj":"PR:P25847"},{"id":"T24","span":{"begin":101,"end":105},"obj":"PR:P43246"},{"id":"T25","span":{"begin":101,"end":105},"obj":"P22711"},{"id":"T26","span":{"begin":101,"end":105},"obj":"PR:P22711"},{"id":"T27","span":{"begin":101,"end":105},"obj":"PR:P54275"},{"id":"T28","span":{"begin":101,"end":105},"obj":"PR:O74773"},{"id":"T29","span":{"begin":101,"end":105},"obj":"PR:P43247"},{"id":"T30","span":{"begin":101,"end":105},"obj":"PR:Q553L4"},{"id":"T31","span":{"begin":101,"end":105},"obj":"PR:O24617"},{"id":"T32","span":{"begin":106,"end":114},"obj":"SO:0000159"},{"id":"T33","span":{"begin":115,"end":123},"obj":"CHEBI:78059"},{"id":"T34","span":{"begin":149,"end":166},"obj":"D015179"},{"id":"T35","span":{"begin":149,"end":166},"obj":"D015179"},{"id":"T36","span":{"begin":276,"end":279},"obj":"GO:0005574"},{"id":"T38","span":{"begin":276,"end":279},"obj":"SO:0000352"},{"id":"T37","span":{"begin":276,"end":279},"obj":"CHEBI:16991"},{"id":"T39","span":{"begin":276,"end":279},"obj":"D004247"},{"id":"T40","span":{"begin":280,"end":295},"obj":"GO:0006298"}],"text":"Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.\nHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, p"}
PubmedHPO
{"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":160,"end":166},"obj":"HP_0002664"},{"id":"T2","span":{"begin":181,"end":201},"obj":"HP_0000006"},{"id":"T3","span":{"begin":181,"end":211},"obj":"HP_0000006"},{"id":"T4","span":{"begin":212,"end":218},"obj":"HP_0002664"}],"text":"Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.\nHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, p"}
UseCases_ArguminSci_Discourse
{"project":"UseCases_ArguminSci_Discourse","denotations":[{"id":"T1","span":{"begin":0,"end":124},"obj":"DRI_Background"}],"text":"Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.\nHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, p"}
DisGeNET
{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":96,"end":100},"obj":"gene:4292"},{"id":"T1","span":{"begin":83,"end":90},"obj":"disease:C0006826"},{"id":"T3","span":{"begin":125,"end":166},"obj":"disease:C1333990"},{"id":"T5","span":{"begin":125,"end":166},"obj":"disease:C1333990"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.\nHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition syndrome caused by germ line mutations in DNA mismatch repair genes, p"}