Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- befree-2016 importedOn "2016-02-19" NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_assertion wasGeneratedBy ECO_0000203 NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_assertion wasDerivedFrom befree-2016 NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_assertion SIO_000772 15071491 NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_assertion evidence source_evidence_literature NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.
- NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_assertion description "[The E148Q variant of MEFV was present in two of the three patients with TNF receptor-associated periodic syndrome (TRAPS) complicated by amyloid in two separate multiplex TRAPS families containing 5 and 16 affected members respectively, and the single patient with Muckle-Wells syndrome who had amyloidosis was homozygous for this variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439026.RAsegseMhC85upms7vXz7xhVqGflwO3UuVf9Jmq_2k-i8130_provenance.