Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- befree-2016 importedOn "2016-02-19" NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_assertion wasGeneratedBy ECO_0000203 NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_assertion wasDerivedFrom befree-2016 NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_assertion SIO_000772 15071491 NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_assertion evidence source_evidence_literature NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.
- NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_assertion description "[We investigated the hypothesis that low-penetrance mutations in genes (TNFRSF1A, MEFV and NALP3/CIAS1) associated with hereditary periodic fever syndromes (HPFs) might be risk factors for AA amyloidosis among patients with chronic inflammatory disorders, including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), Crohn's disease, undiagnosed recurrent fevers and HPFs themselves.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439030.RAujq7TWfp4UH7kGoBRF5WKfNXJj_yJfsX_PcEoHLj75I130_provenance.