PubMed:18223211
Annnotations
c_corpus
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T3 | 0-24 | D002285 | denotes | Ductal carcinoma in situ |
T4 | 0-24 | D002285 | denotes | Ductal carcinoma in situ |
T9 | 63-69 | UBERON:0000310 | denotes | breast |
T10 | 63-76 | D001943 | denotes | breast cancer |
T11 | 63-76 | D001943 | denotes | breast cancer |
T12 | 97-102 | D006801 | denotes | Human |
T13 | 112-118 | UBERON:0000310 | denotes | breast |
T14 | 119-126 | D009369 | denotes | cancers |
T15 | 119-126 | D009369 | denotes | cancers |
T16 | 128-131 | CVCL_EQ33 | denotes | IBC |
T19 | 234-258 | D002285 | denotes | ductal carcinoma in situ |
T20 | 234-258 | D002285 | denotes | ductal carcinoma in situ |
T26 | 260-264 | CVCL_5552 | denotes | DCIS |
T25 | 260-264 | D002285 | denotes | DCIS |
T27 | 260-264 | D002285 | denotes | DCIS |
T28 | 404-414 | D015415 | denotes | biomarkers |
T29 | 404-414 | D015415 | denotes | biomarkers |
T30 | 477-481 | PR:Q8FYW3 | denotes | pure |
T31 | 477-481 | PR:Q54QE4 | denotes | pure |
T32 | 477-481 | PR:P52558 | denotes | pure |
T33 | 477-481 | PR:P0AG18 | denotes | pure |
T35 | 477-481 | PR:000023640 | denotes | pure |
T34 | 477-481 | GO:0034023 | denotes | pure |
T37 | 482-486 | CVCL_5552 | denotes | DCIS |
T36 | 482-486 | D002285 | denotes | DCIS |
T38 | 482-486 | D002285 | denotes | DCIS |
T40 | 571-575 | CVCL_5552 | denotes | DCIS |
T39 | 571-575 | D002285 | denotes | DCIS |
T41 | 571-575 | D002285 | denotes | DCIS |
T43 | 602-605 | GO:0005574 | denotes | DNA |
T45 | 602-605 | SO:0000352 | denotes | DNA |
T44 | 602-605 | CHEBI:16991 | denotes | DNA |
T46 | 602-605 | D004247 | denotes | DNA |
T47 | 638-645 | D010634 | denotes | luminal |
T48 | 638-645 | D010634 | denotes | luminal |
T49 | 638-645 | CHEBI:8069 | denotes | luminal |
T52 | 658-663 | PR:P70424 | denotes | erbB2 |
T53 | 658-663 | PR:P06494 | denotes | erbB2 |
T54 | 658-663 | PR:P04626 | denotes | erbB2 |
T55 | 658-663 | PR:000002082 | denotes | erbB2 |
T57 | 735-739 | CVCL_5552 | denotes | DCIS |
T56 | 735-739 | D002285 | denotes | DCIS |
T58 | 735-739 | D002285 | denotes | DCIS |
T59 | 852-862 | D015415 | denotes | biomarkers |
T60 | 852-862 | D015415 | denotes | biomarkers |
T62 | 962-966 | CVCL_5552 | denotes | DCIS |
T61 | 962-966 | D002285 | denotes | DCIS |
T63 | 962-966 | D002285 | denotes | DCIS |
T64 | 1042-1052 | D015415 | denotes | biomarkers |
T65 | 1042-1052 | D015415 | denotes | biomarkers |
T67 | 1173-1177 | CVCL_5552 | denotes | DCIS |
T66 | 1173-1177 | D002285 | denotes | DCIS |
T68 | 1173-1177 | D002285 | denotes | DCIS |
T69 | 1266-1275 | CHEBI:59163 | denotes | biomarker |
T71 | 1341-1345 | CVCL_5552 | denotes | DCIS |
T70 | 1341-1345 | D002285 | denotes | DCIS |
T72 | 1341-1345 | D002285 | denotes | DCIS |
T74 | 1431-1435 | CVCL_5552 | denotes | DCIS |
T73 | 1431-1435 | D002285 | denotes | DCIS |
T75 | 1431-1435 | D002285 | denotes | DCIS |
T76 | 1471-1474 | PR:P04637 | denotes | p53 |
T77 | 1471-1474 | PR:000003035 | denotes | p53 |
T78 | 1471-1474 | PR:P02340 | denotes | p53 |
T79 | 1471-1474 | PR:Q42578 | denotes | p53 |
T80 | 1471-1474 | PR:P10361 | denotes | p53 |
T82 | 1566-1570 | CVCL_5552 | denotes | DCIS |
T81 | 1566-1570 | D002285 | denotes | DCIS |
T83 | 1566-1570 | D002285 | denotes | DCIS |
T85 | 1613-1617 | CVCL_5552 | denotes | DCIS |
T84 | 1613-1617 | D002285 | denotes | DCIS |
T86 | 1613-1617 | D002285 | denotes | DCIS |
T87 | 1789-1792 | PR:P04637 | denotes | p53 |
T88 | 1789-1792 | PR:000003035 | denotes | p53 |
T89 | 1789-1792 | PR:P02340 | denotes | p53 |
T90 | 1789-1792 | PR:Q42578 | denotes | p53 |
T91 | 1789-1792 | PR:P10361 | denotes | p53 |
T92 | 1793-1801 | SO:0000109 | denotes | mutation |
T93 | 1842-1845 | CVCL_EQ33 | denotes | IBC |
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T0 | 658-663 | gene:2064 | denotes | erbB2 |
T1 | 571-575 | disease:C0007124 | denotes | DCIS |
R1 | T0 | T1 | associated_with | erbB2,DCIS |
UseCases_ArguminSci_Discourse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-87 | DRI_Background | denotes | Ductal carcinoma in situ and the emergence of diversity during breast cancer evolution. |
T2 | 97-183 | DRI_Background | denotes | Human invasive breast cancers (IBC) show enormous histologic and biological diversity. |
T3 | 184-300 | DRI_Background | denotes | This study comprehensively evaluated diversity in ductal carcinoma in situ (DCIS), the immediate precursors of IBCs. |
T4 | 322-554 | DRI_Background | denotes | The extent of diversity for conventional histologic grade and standard prognostic biomarkers assessed by immunohistochemistry was evaluated in a series of pure DCIS (n = 200) compared with a contemporaneous series of IBCs (n = 200). |
T5 | 555-683 | DRI_Approach | denotes | A subset of the DCIS (n = 25) was evaluated by DNA microarrays for the presence of luminal, basal, and erbB2 intrinsic subtypes. |
T6 | 684-952 | DRI_Approach | denotes | The extent of diversity within individual cases of DCIS (n = 120) was determined by assessing multiple regions independently for histologic (nuclear) grade and several biomarkers by immunohistochemistry, which approximate microarrays in determining intrinsic subtypes. |
T7 | 962-1122 | DRI_Background | denotes | DCIS showed a broad distribution of conventional histologic grades and standard biomarkers ranging from well to poorly differentiated, nearly identical to IBCs. |
T8 | 1123-1189 | DRI_Outcome | denotes | Microarrays showed the same intrinsic subtypes in DCIS as in IBCs. |
T9 | 1190-1404 | DRI_Outcome | denotes | However, higher resolution analysis showed that multiple histologic grades, biomarker phenotypes, and intrinsic subtypes often coexist within the same DCIS, and these diverse regions probably compete for dominance. |
T10 | 1405-1488 | DRI_Background | denotes | Diversity within cases of DCIS was highly correlated with mutated p53 (P = 0.0007). |
T11 | 1502-1709 | DRI_Background | denotes | These results support the hypothesis that poorly differentiated DCIS gradually evolve from well-differentiated DCIS by randomly acquiring genetic defects resulting in increasingly abnormal cellular features. |
T12 | 1710-1897 | DRI_Background | denotes | This diversity is amplified by defects resulting in genetic instability (e.g., p53 mutation), and the alterations are propagated to IBC in a manner independent of progression to invasion. |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
18223211-4#103#108#gene2064 | 658-663 | gene2064 | denotes | erbB2 |
18223211-4#16#20#diseaseC0007124 | 571-575 | diseaseC0007124 | denotes | DCIS |
18223211-9#66#69#gene7157 | 1471-1474 | gene7157 | denotes | p53 |
18223211-9#26#30#diseaseC0007124 | 1431-1435 | diseaseC0007124 | denotes | DCIS |
103#108#gene206416#20#diseaseC0007124 | 18223211-4#103#108#gene2064 | 18223211-4#16#20#diseaseC0007124 | associated_with | erbB2,DCIS |
66#69#gene715726#30#diseaseC0007124 | 18223211-9#66#69#gene7157 | 18223211-9#26#30#diseaseC0007124 | associated_with | p53,DCIS |