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PubMed:11851721 JSONTXT 9 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
11851721-0#0#4#gene5444 207-211 gene5444 denotes PON1
11851721-2#55#72#diseaseC0242231 435-452 diseaseC0242231 denotes coronary stenosis
11851721-2#82#105#diseaseC0010054 462-485 diseaseC0010054 denotes coronary artery disease
11851721-2#82#105#diseaseC0010068 462-485 diseaseC0010068 denotes coronary artery disease
11851721-2#82#105#diseaseC1956346 462-485 diseaseC1956346 denotes coronary artery disease
11851721-2#82#105#diseaseC0010054 462-485 diseaseC0010054 denotes coronary artery disease
11851721-2#82#105#diseaseC0010068 462-485 diseaseC0010068 denotes coronary artery disease
11851721-2#82#105#diseaseC1956346 462-485 diseaseC1956346 denotes coronary artery disease
11851721-2#116#119#gene790 496-499 gene790 denotes CAD
11851721-2#116#119#gene790 496-499 gene790 denotes CAD
11851721-2#184#187#gene790 564-567 gene790 denotes CAD
11851721-2#184#187#gene790 564-567 gene790 denotes CAD
11851721-0#45#69#diseaseC0010054 643-1214 diseaseC0010054 denotes chain reaction and restriction enzyme digestion. RESULTS: In the pooled population, the frequencies of L and M alleles were 0.63 and 0.37, respectively; the most common haplotypes were QQ/LM (24.2%) and QR/LL (21.8%) and a strong linkage disequilibrium between L/55 and R/192 alleles was observed (D' = -0.91; P < 0.0001). CAD+ subjects did not show any significant differences in the distribution of PON1-55 genotypes as compared to CAD- subjects and population controls (chi2 = 1.5, P = 0.8). After controlling for other risk factors, the low-concentration M allele was
11851721-10#80#84#gene5444 2092-2096 gene5444 denotes PON1
11851721-10#113#134#diseaseC0027051 2125-2146 diseaseC0027051 denotes myocardial infarction
0#4#gene544445#69#diseaseC0010054 11851721-0#0#4#gene5444 11851721-0#45#69#diseaseC0010054 associated_with PON1,"chain reaction and restriction enzyme digestion. RESULTS: In the pooled population, the frequencies of L and M alleles were 0.63 and 0.37, respectively; the most common haplotypes were QQ/LM (24.2%) and QR/LL (21.8%) and a strong linkage disequilibrium between L/55 and R/192 alleles was observed (D' = -0.91; P < 0.0001). CAD+ subjects did not show any significant differences in the distribution of PON1-55 genotypes as compared to CAD- subjects and population controls (chi2 = 1.5, P = 0.8). After controlling for other risk factors, the low-concentration M allele was"
116#119#gene79055#72#diseaseC0242231 11851721-2#116#119#gene790 11851721-2#55#72#diseaseC0242231 associated_with CAD,coronary stenosis
116#119#gene79055#72#diseaseC0242231 11851721-2#116#119#gene790 11851721-2#55#72#diseaseC0242231 associated_with CAD,coronary stenosis
116#119#gene79082#105#diseaseC0010054 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010054 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010054 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010054 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010068 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010068 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010068 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC0010068 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC1956346 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC1956346 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC1956346 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
116#119#gene79082#105#diseaseC1956346 11851721-2#116#119#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
184#187#gene79055#72#diseaseC0242231 11851721-2#184#187#gene790 11851721-2#55#72#diseaseC0242231 associated_with CAD,coronary stenosis
184#187#gene79055#72#diseaseC0242231 11851721-2#184#187#gene790 11851721-2#55#72#diseaseC0242231 associated_with CAD,coronary stenosis
184#187#gene79082#105#diseaseC0010054 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010054 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010054 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010054 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010054 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010068 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010068 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010068 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC0010068 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC0010068 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC1956346 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC1956346 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC1956346 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
184#187#gene79082#105#diseaseC1956346 11851721-2#184#187#gene790 11851721-2#82#105#diseaseC1956346 associated_with CAD,coronary artery disease
80#84#gene5444113#134#diseaseC0027051 11851721-10#80#84#gene5444 11851721-10#113#134#diseaseC0027051 associated_with PON1,myocardial infarction