Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_assertion description "[Overall, those data strongly suggest that the GLA p.(Arg118Cys) variant does not segregate with FD clinical phenotypes in a Mendelian fashion, but might be a modulator of the multifactorial risk of cerebrovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_assertion evidence source_evidence_literature NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_assertion SIO_000772 25468652 NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_assertion wasDerivedFrom befree-2016 NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_assertion wasGeneratedBy ECO_0000203 NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244297.RA9Ba5h_5rM2II6OfSnofXiSk5ZZsR0BDMc1CEzMRUGBQ130_provenance.