Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_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." NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_assertion evidence source_evidence_literature NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_assertion SIO_000772 20378690 NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_assertion wasDerivedFrom gad-20130706 NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_assertion wasGeneratedBy ECO_0000203 NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP92411.RApsyP5T9FInXLZyctnxu3k09vlk9NxsjhxwltZDcsEtU130_provenance.