PubMed:16371368 / 1290-1489 JSONTXT

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sonoma2

Id Subject Object Predicate Lexical cue
T-46 30-43 VAR denotes E76K mutation
T-47 44-50 REG denotes caused
T-48 51-77 DISEASE denotes myeloproliferative disease
T-49 120-129 NEGREG denotes decreased
T-50 130-153 CPA denotes hematopoietic potential
R-57 T-46 T-49 CauseOf E76K mutation,decreased
R-58 T-48 T-47 ThemeOf myeloproliferative disease,caused
R-59 T-50 T-49 ThemeOf hematopoietic potential,decreased
R-56 T-46 T-47 CauseOf E76K mutation,caused

sonoma

Id Subject Object Predicate Lexical cue
T-48 24-29 GENE denotes SHP-2
T-49 30-43 VAR denotes E76K mutation
T-50 44-50 REG denotes caused
T-51 51-77 DISEASE denotes myeloproliferative disease
T-52 114-119 GENE denotes SHP-2
T-53 120-129 NEGREG denotes decreased
T-54 130-153 CPA denotes hematopoietic potential
R-88 T-48 T-49 ThemeOf SHP-2,E76K mutation
R-89 T-48 T-51 A SHP-2,myeloproliferative disease
R-90 T-49 T-50 CauseOf E76K mutation,caused
R-91 T-49 T-53 CauseOf E76K mutation,decreased
R-92 T-50 T-51 ThemeOf caused,myeloproliferative disease
R-93 T-52 T-53 ThemeOf SHP-2,decreased
R-94 T-53 T-54 ThemeOf decreased,hematopoietic potential

sentences

Id Subject Object Predicate Lexical cue
T8 0-199 Sentence denotes Our results showed that SHP-2 E76K mutation caused myeloproliferative disease in mice, while overexpression of WT SHP-2 decreased hematopoietic potential of the transduced cells in recipient animals.

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
16371368-7#30#34#geners121918464 30-34 geners121918464 denotes E76K
16371368-7#51#77#diseaseC0027022 51-77 diseaseC0027022 denotes myeloproliferative disease
30#34#geners12191846451#77#diseaseC0027022 16371368-7#30#34#geners121918464 16371368-7#51#77#diseaseC0027022 associated_with E76K,myeloproliferative disease

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
16371368-7#24#29#gene5781 24-29 gene5781 denotes SHP-2
16371368-7#114#119#gene5781 114-119 gene5781 denotes SHP-2
16371368-7#51#77#diseaseC0027022 51-77 diseaseC0027022 denotes myeloproliferative disease
24#29#gene578151#77#diseaseC0027022 16371368-7#24#29#gene5781 16371368-7#51#77#diseaseC0027022 associated_with SHP-2,myeloproliferative disease
114#119#gene578151#77#diseaseC0027022 16371368-7#114#119#gene5781 16371368-7#51#77#diseaseC0027022 associated_with SHP-2,myeloproliferative disease

kaiyin_test

Id Subject Object Predicate Lexical cue
T10 24-29 Gene denotes SHP-2
T11 30-43 Var denotes E76K mutation
T12 51-85 Disease denotes myeloproliferative disease in mice
R5 T10 T11 ThemeOf SHP-2,E76K mutation
R6 T11 T12 CauseOf E76K mutation,myeloproliferative disease in mice

name_no

Id Subject Object Predicate Lexical cue
T10 24-29 Gene denotes SHP-2
T11 30-43 Var denotes E76K mutation
T12 51-85 Disease denotes myeloproliferative disease in mice
R5 T10 T11 ThemeOf SHP-2,E76K mutation
R6 T11 T12 CauseOf E76K mutation,myeloproliferative disease in mice

NCBITAXON

Id Subject Object Predicate Lexical cue db_id
T2 81-85 OrganismTaxon denotes mice 10088