Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_assertion description "[The results of this study suggest that MEFV gene mutations appear to be an aggravating factor for the severity of RA, and consequently, patients with RA might be screened for MEFV gene mutations in countries where FMF is frequent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_assertion evidence source_evidence_literature NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_assertion SIO_000772 20031469 NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_assertion wasDerivedFrom gad-20130706 NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_assertion wasGeneratedBy ECO_0000203 NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP69949.RATWbcVlRpyrW5rI2KIAM5NAf5K9vcYKmtIGlkPAbNfwk130_provenance.