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- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion type Assertion NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_head.
- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion wasGeneratedBy ECO_0000203 NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_provenance.
- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion wasDerivedFrom befree-2016 NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_provenance.
- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion SIO_000772 16799619 NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_provenance.
- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion evidence source_evidence_literature NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_provenance.
- NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_assertion description "[The second set of genetic alterations are etiological nonspecific, it includes recurrent gains and losses of chromosomes, alteration of TP53 gene, activation of WNT/beta-catenin pathway through CTNNB1/beta-catenin and AXIN (axis inhibition protein) mutations, inactivation of retinoblastoma and IGF2R (insulin-like growth factor 2 receptor) pathways through inactivation of RB1 (retinoblastoma 1), P16 and IGF2R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556463.RAe_VBv2cNBP3w0ema6865gaXav-vT8-oP4GluAal8yrk130_provenance.