Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion> ?p ?o ?g. }
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- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion type Assertion NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_head.
- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion wasGeneratedBy ECO_0000203 NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_provenance.
- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion wasDerivedFrom befree-2016 NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_provenance.
- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion SIO_000772 15071491 NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_provenance.
- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_assertion evidence source_evidence_literature NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_provenance.
- NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_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." NP439031.RA6IVjNsZE5BfYuNz9m2bms4oV0tkkHCHdpkW-1XCNmcM130_provenance.