Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_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." NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_assertion evidence source_evidence_literature NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_assertion SIO_000772 18434448 NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_assertion wasDerivedFrom gad-20150221 NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_assertion wasGeneratedBy ECO_0000203 NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90464.RAKydtpMxhE4SrsLWx0CggdjKHDGNtau8bD0N19sf6DRA130_provenance.