Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_assertion description "[Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_assertion evidence source_evidence_literature NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_assertion SIO_000772 17914026 NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_assertion wasDerivedFrom lhgdn-20090331 NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_assertion wasGeneratedBy ECO_0000203 NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP148972.RAAc2oLfDHOU7IWGiAZSJEHcVOY3dx_sxn2-7s6YdNxoU130_provenance.