Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- befree-2016 importedOn "2016-02-19" NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_assertion wasGeneratedBy ECO_0000203 NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_assertion wasDerivedFrom befree-2016 NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_assertion SIO_000772 15071491 NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_assertion evidence source_evidence_literature NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.
- NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_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." NP439022.RAOQT2IbNVmS0MdEFZZLBBGl6fqgiKVRR1_5K8wP2yVng130_provenance.