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- source_evidence_literature type ECO_0000212 NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_assertion description "[This study analysed 12 single-nucleotide polymorphisms (SNPs) in selenoprotein genes [glutathione peroxidase 1 (GPX1), GPX4, 15 kDa selenoprotein (SEP15), selenoprotein S (SELS), selenoprotein P (SEPP1) and thioredoxin reductase 2 (TXNRD2)] and in genes that code for a key protein in Se incorporation [SECIS-binding protein 2 (SBP2)] and in antioxidant defence [superoxide dismutase 2 (SOD2)] in relation to sporadic CRC incidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_assertion evidence source_evidence_literature NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_assertion SIO_000772 20378690 NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_assertion wasDerivedFrom befree-20140225 NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_assertion wasGeneratedBy ECO_0000203 NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717429.RAgB5HygHDgXxC9VRmcyZCfHPi3lzZXmf1a2Ua2bG8gXw130_provenance.