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- source_evidence_literature type ECO_0000212 NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_assertion description "[Neither the VDR C352T nor the MPO G463A genotype had manifested association with the dysplasia and carcinoma of the disease, whereas the MTHFR 677TT genotype may be a genetic risk factor for esophageal dysplasia and carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_assertion evidence source_evidence_literature NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_assertion SIO_000772 18662591 NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_assertion wasDerivedFrom gad-20150221 NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_assertion wasGeneratedBy ECO_0000203 NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP119961.RAeHGZVP_mLqnDu_WWoDFtCMDcm0QfI7e3_MgeLULtJj4130_provenance.