PubMed:16371368 / 1290-1489 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/16371368","sourcedb":"PubMed","sourceid":"16371368","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/16371368","text":"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.","tracks":[{"project":"sonoma2","denotations":[{"id":"T-46","span":{"begin":30,"end":43},"obj":"VAR"},{"id":"T-47","span":{"begin":44,"end":50},"obj":"REG"},{"id":"T-48","span":{"begin":51,"end":77},"obj":"DISEASE"},{"id":"T-49","span":{"begin":120,"end":129},"obj":"NEGREG"},{"id":"T-50","span":{"begin":130,"end":153},"obj":"CPA"}],"relations":[{"id":"R-57","pred":"CauseOf","subj":"T-46","obj":"T-49"},{"id":"R-58","pred":"ThemeOf","subj":"T-48","obj":"T-47"},{"id":"R-59","pred":"ThemeOf","subj":"T-50","obj":"T-49"},{"id":"R-56","pred":"CauseOf","subj":"T-46","obj":"T-47"}],"attributes":[{"subj":"T-46","pred":"source","obj":"sonoma2"},{"subj":"T-47","pred":"source","obj":"sonoma2"},{"subj":"T-48","pred":"source","obj":"sonoma2"},{"subj":"T-49","pred":"source","obj":"sonoma2"},{"subj":"T-50","pred":"source","obj":"sonoma2"}]},{"project":"sonoma","denotations":[{"id":"T-48","span":{"begin":24,"end":29},"obj":"GENE"},{"id":"T-49","span":{"begin":30,"end":43},"obj":"VAR"},{"id":"T-50","span":{"begin":44,"end":50},"obj":"REG"},{"id":"T-51","span":{"begin":51,"end":77},"obj":"DISEASE"},{"id":"T-52","span":{"begin":114,"end":119},"obj":"GENE"},{"id":"T-53","span":{"begin":120,"end":129},"obj":"NEGREG"},{"id":"T-54","span":{"begin":130,"end":153},"obj":"CPA"}],"relations":[{"id":"R-88","pred":"ThemeOf","subj":"T-48","obj":"T-49"},{"id":"R-89","pred":"A","subj":"T-48","obj":"T-51"},{"id":"R-90","pred":"CauseOf","subj":"T-49","obj":"T-50"},{"id":"R-91","pred":"CauseOf","subj":"T-49","obj":"T-53"},{"id":"R-92","pred":"ThemeOf","subj":"T-50","obj":"T-51"},{"id":"R-93","pred":"ThemeOf","subj":"T-52","obj":"T-53"},{"id":"R-94","pred":"ThemeOf","subj":"T-53","obj":"T-54"}],"attributes":[{"subj":"T-48","pred":"source","obj":"sonoma"},{"subj":"T-49","pred":"source","obj":"sonoma"},{"subj":"T-50","pred":"source","obj":"sonoma"},{"subj":"T-51","pred":"source","obj":"sonoma"},{"subj":"T-52","pred":"source","obj":"sonoma"},{"subj":"T-53","pred":"source","obj":"sonoma"},{"subj":"T-54","pred":"source","obj":"sonoma"}]},{"project":"sentences","denotations":[{"id":"T8","span":{"begin":0,"end":199},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"T8","pred":"source","obj":"sentences"}]},{"project":"DisGeNET5_variant_disease","denotations":[{"id":"16371368-7#30#34#geners121918464","span":{"begin":30,"end":34},"obj":"geners121918464"},{"id":"16371368-7#51#77#diseaseC0027022","span":{"begin":51,"end":77},"obj":"diseaseC0027022"}],"relations":[{"id":"30#34#geners12191846451#77#diseaseC0027022","pred":"associated_with","subj":"16371368-7#30#34#geners121918464","obj":"16371368-7#51#77#diseaseC0027022"}],"attributes":[{"subj":"16371368-7#30#34#geners121918464","pred":"source","obj":"DisGeNET5_variant_disease"},{"subj":"16371368-7#51#77#diseaseC0027022","pred":"source","obj":"DisGeNET5_variant_disease"}]},{"project":"DisGeNET5_gene_disease","denotations":[{"id":"16371368-7#24#29#gene5781","span":{"begin":24,"end":29},"obj":"gene5781"},{"id":"16371368-7#114#119#gene5781","span":{"begin":114,"end":119},"obj":"gene5781"},{"id":"16371368-7#51#77#diseaseC0027022","span":{"begin":51,"end":77},"obj":"diseaseC0027022"}],"relations":[{"id":"24#29#gene578151#77#diseaseC0027022","pred":"associated_with","subj":"16371368-7#24#29#gene5781","obj":"16371368-7#51#77#diseaseC0027022"},{"id":"114#119#gene578151#77#diseaseC0027022","pred":"associated_with","subj":"16371368-7#114#119#gene5781","obj":"16371368-7#51#77#diseaseC0027022"}],"attributes":[{"subj":"16371368-7#24#29#gene5781","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"16371368-7#114#119#gene5781","pred":"source","obj":"DisGeNET5_gene_disease"},{"subj":"16371368-7#51#77#diseaseC0027022","pred":"source","obj":"DisGeNET5_gene_disease"}]},{"project":"kaiyin_test","denotations":[{"id":"T10","span":{"begin":24,"end":29},"obj":"Gene"},{"id":"T11","span":{"begin":30,"end":43},"obj":"Var"},{"id":"T12","span":{"begin":51,"end":85},"obj":"Disease"}],"relations":[{"id":"R5","pred":"ThemeOf","subj":"T10","obj":"T11"},{"id":"R6","pred":"CauseOf","subj":"T11","obj":"T12"}],"attributes":[{"subj":"T10","pred":"source","obj":"kaiyin_test"},{"subj":"T11","pred":"source","obj":"kaiyin_test"},{"subj":"T12","pred":"source","obj":"kaiyin_test"}]},{"project":"name_no","denotations":[{"id":"T10","span":{"begin":24,"end":29},"obj":"Gene"},{"id":"T11","span":{"begin":30,"end":43},"obj":"Var"},{"id":"T12","span":{"begin":51,"end":85},"obj":"Disease"}],"relations":[{"id":"R5","pred":"ThemeOf","subj":"T10","obj":"T11"},{"id":"R6","pred":"CauseOf","subj":"T11","obj":"T12"}],"attributes":[{"subj":"T10","pred":"source","obj":"name_no"},{"subj":"T11","pred":"source","obj":"name_no"},{"subj":"T12","pred":"source","obj":"name_no"}]},{"project":"NCBITAXON","denotations":[{"id":"T2","span":{"begin":81,"end":85},"obj":"OrganismTaxon"}],"attributes":[{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"subj":"T2","pred":"source","obj":"NCBITAXON"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sonoma2","color":"#94ec93","default":true},{"id":"sonoma","color":"#ec93ae"},{"id":"sentences","color":"#93c8ec"},{"id":"DisGeNET5_variant_disease","color":"#e2ec93"},{"id":"DisGeNET5_gene_disease","color":"#dc93ec"},{"id":"kaiyin_test","color":"#93ecc1"},{"id":"name_no","color":"#eca793"},{"id":"NCBITAXON","color":"#9398ec"}]}]}}