| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-36 |
Sentence |
denotes |
MUC1 in carcinoma-host interactions. |
| T1 |
0-36 |
Sentence |
denotes |
MUC1 in carcinoma-host interactions. |
| TextSentencer_T2 |
37-149 |
Sentence |
denotes |
Many carcinoma-associated markers are glycoconjugates whose expression undergoes temporal or spatial regulation. |
| T2 |
37-149 |
Sentence |
denotes |
Many carcinoma-associated markers are glycoconjugates whose expression undergoes temporal or spatial regulation. |
| TextSentencer_T3 |
150-374 |
Sentence |
denotes |
Mucin-1 (MUC1), discovered through monoclonal antibody technology, is a well-documented example of such a molecule and influences numerous pathophysiological behaviors, such as the invasion and metastasis of carcinoma cells. |
| T3 |
150-374 |
Sentence |
denotes |
Mucin-1 (MUC1), discovered through monoclonal antibody technology, is a well-documented example of such a molecule and influences numerous pathophysiological behaviors, such as the invasion and metastasis of carcinoma cells. |
| TextSentencer_T4 |
375-527 |
Sentence |
denotes |
Levels of MUC1 expression in carcinomas correlate with the clinical stage of the cancer and inversely correlate with the survival prospects of patients. |
| T4 |
375-527 |
Sentence |
denotes |
Levels of MUC1 expression in carcinomas correlate with the clinical stage of the cancer and inversely correlate with the survival prospects of patients. |
| TextSentencer_T5 |
528-624 |
Sentence |
denotes |
The MUC1 immune response is known to provide a protective host defense mechanism against cancer. |
| T5 |
528-624 |
Sentence |
denotes |
The MUC1 immune response is known to provide a protective host defense mechanism against cancer. |
| TextSentencer_T6 |
625-789 |
Sentence |
denotes |
The multiple functions of MUC1 in carcinoma-host interactions are believed to be dependent on the polymorphic nature of MUC1, particularly its glycosylation status. |
| T6 |
625-789 |
Sentence |
denotes |
The multiple functions of MUC1 in carcinoma-host interactions are believed to be dependent on the polymorphic nature of MUC1, particularly its glycosylation status. |