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- source_evidence_literature type ECO_0000212 NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_assertion description "[Single locus analysis by logistic regression showed association of MSH2 IVS1+9G>C (rs2303426), ERCC2 Asp312Asn (rs1799793), OGG1 Ser326Cys (rs1052133), OGG1 IVS4-15C>G (rs2072668), CASP8 -652 6N ins/del (rs3834129), PTGS2 -1195G>A (rs689466), PTGS2 -765G>C (rs20417), TLR4 Ex4+936C>T (rs4986791) and TLR2 -196 to -174del polymorphisms with GBC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_assertion evidence source_evidence_literature NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_assertion SIO_000772 21283657 NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_assertion wasDerivedFrom befree-2016 NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_assertion wasGeneratedBy ECO_0000203 NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.
- befree-2016 importedOn "2016-02-19" NP869205.RA_sc4A_ad1BSBqwqNTDXPCNapf-WWay2y6ld8tY8b-MY130_provenance.