Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_assertion wasGeneratedBy ECO_0000203 NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_assertion wasDerivedFrom befree-2016 NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_assertion SIO_000772 15071491 NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_assertion evidence source_evidence_literature NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.
- NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_assertion description "[Although allelic variants in HPFs genes are not major susceptibility factors for AA amyloidosis in chronic inflammatory disease, low-penetrance variants of MEFV and TNFRSF1A may have clinically significant proinflammatory effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439028.RAuuGVWo2V7uEv402xcGQhIppZhG8qXiNVktda42SMKhQ130_provenance.