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- source_evidence_literature type ECO_0000212 NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_assertion description "[Large meta-analyses confirmed the association between IL8, IL10, TNF-b, TP53 and PSCA, while genetic variation at different genes such as XPG, PLCE1, HFE, ERCC5, EZH2, DOC2, CYP19A1, ALDH2, and CDH1 have been reported to be associated with GC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_assertion evidence source_evidence_literature NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_assertion SIO_000772 24011243 NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_assertion wasDerivedFrom befree-2016 NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_assertion wasGeneratedBy ECO_0000203 NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108157.RAWaliIdeMiomr95yxxcol-8en2IHoicBs_3a0oW3-8Dw130_provenance.