Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_assertion description "[It is most frequently seen in patients with hereditary transthyretin (TTR) amyloidosis, but is also present in 20% of patients with systemic immunoglobulin light chain (primary) amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_assertion evidence source_evidence_literature NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_assertion SIO_000772 17554795 NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_assertion wasDerivedFrom befree-2016 NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_assertion wasGeneratedBy ECO_0000203 NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.
- befree-2016 importedOn "2016-02-19" NP614023.RAwaifiiqUDVTgnoqXtW5RIF_Tu3QK3cduwE-I-HyTsXA130_provenance.