Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion> ?p ?o ?g. }
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- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion type Assertion NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_head.
- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion description "[Hyperactive mTOR signaling due to the loss-of-function of mutations in either TSC1 or TSC2 gene causes TSC, an autosomal dominant disorder featured with benign tumors in multiple organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_provenance.
- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion evidence source_evidence_literature NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_provenance.
- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion SIO_000772 23108404 NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_provenance.
- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion wasDerivedFrom befree-20140225 NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_provenance.
- NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_assertion wasGeneratedBy ECO_0000203 NP651415.RAwz5mhC5o_P0x74gPKNF4yzpbAQEg_WLdpfCYpFbrmpM130_provenance.