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- source_evidence_literature type ECO_0000212 NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_assertion description "[A high prevalence of genetic alterations in PI3K/AKT pathway in Saudi cohort of CRC, predominance of PIK3CA mutations in the MSI subgroup and their possible involvement in development/progression of this subset of CRC are some of the significant findings of our study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_assertion evidence source_evidence_literature NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_assertion SIO_000772 18193083 NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_assertion wasDerivedFrom befree-2016 NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_assertion wasGeneratedBy ECO_0000203 NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.
- befree-2016 importedOn "2016-02-19" NP649752.RAnF7dnw9gP-uEz6V_hH_RfUPOruM0AKv9fO3CaG74RfY130_provenance.