Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_assertion description "[A total of 181 single nucleotide polymorphisms (SNPs) uniformly spaced along the genomic sequences of 17 core genes of the NFkappaB pathway (REL, RELA, RELB, NFKB1, NFKB2, NFKBIA, NFKBIB, NFKBIE, IKBKA, IKBKB, IKBKE, IKBKAP, KBRAS1, KBRAS2, MAP3K1, MAP3K14, TAX1BP1) were studied by mass spectrometry analysis complemented with 5'-nuclease fluorescence assays in the discovery set, 458 patients with RA and 657 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_assertion evidence source_evidence_literature NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_assertion SIO_000772 18434448 NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_assertion wasDerivedFrom gad-20150221 NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_assertion wasGeneratedBy ECO_0000203 NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP122179.RAiEyW3ExgMqp1cvi4QJfJt-go0DWJajMt28Xe0p5FmKg130_provenance.