Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_assertion description "[We observed an accumulation of rare nonsynonymous variants exclusive to RA cases in IL2RA and IL2RB (burden test: p = 0.007 and p = 0.018, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_assertion evidence source_evidence_literature NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_assertion SIO_000772 23261300 NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_assertion wasDerivedFrom befree-2016 NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_assertion wasGeneratedBy ECO_0000203 NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1038003.RARLMtIr_4-cwnfLKcbWqc--QRFgyiTZMk_Bb-rlLsr0s130_provenance.