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PubMed:24808909 JSONTXT

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sonoma2

Id Subject Object Predicate Lexical cue
T0 40-44 NEGREG denotes loss
T1 57-65 VAR denotes variants
T2 246-254 VAR denotes variants
T3 277-284 REG denotes results
T4 288-304 NEGREG denotes loss of function
T5 373-381 VAR denotes variants
T6 691-721 DISEASE denotes hypocholesterolemia-associated
T7 722-725 NEGREG denotes LOF
T8 726-735 VAR denotes mutations
T9 743-748 GENE denotes PCSK9
R0 T1 T0 CauseOf variants,loss
R1 T2 T3 CauseOf variants,results
R2 T2 T4 CauseOf variants,loss of function
R3 T6 T7 ThemeOf hypocholesterolemia-associated,LOF
R4 T6 T8 ThemeOf hypocholesterolemia-associated,mutations
R5 T8 T7 CauseOf mutations,LOF
R6 T9 T8 ThemeOf PCSK9,mutations

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 691-710 HP_0003146 denotes hypocholesterolemia

Allie

Id Subject Object Predicate Lexical cue
SS1_24808909_1_0 288-304 expanded denotes loss of function
SS2_24808909_1_0 306-309 abbr denotes LOF
SS1_24808909_3_0 570-608 expanded denotes electronic medical record and genomics
SS2_24808909_3_0 610-616 abbr denotes eMERGE
AE1_24808909_1_0 SS1_24808909_1_0 SS2_24808909_1_0 abbreviatedTo loss of function,LOF
AE1_24808909_3_0 SS1_24808909_3_0 SS2_24808909_3_0 abbreviatedTo electronic medical record and genomics,eMERGE

kaiyin_test

Id Subject Object Predicate Lexical cue
T7 691-710 Disease denotes hypocholesterolemia
T6 722-725 NegReg denotes LOF
T4 726-735 Var denotes mutations
T5 743-748 Gene denotes PCSK9
R3 T4 T6 CauseOf mutations,LOF
R4 T7 T6 ThemeOf hypocholesterolemia,LOF
R5 T5 T4 ThemeOf PCSK9,mutations

name_no

Id Subject Object Predicate Lexical cue
T7 691-710 Disease denotes hypocholesterolemia
T6 722-725 NegReg denotes LOF
T4 726-735 Var denotes mutations
T5 743-748 Gene denotes PCSK9
R3 T4 T6 CauseOf mutations,LOF
R4 T7 T6 ThemeOf hypocholesterolemia,LOF
R5 T5 T4 ThemeOf PCSK9,mutations