Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_assertion description "[We analyzed the frequency of single-nucleotide polymorphisms (SNPs) in genes encoding CCL2 (-2518 and -2076) and CCL5 (-403 and -28) in patients with Beh�et's disease (BD), a systemic form of uveitis, and patients with retinal vasculitis (RV), an organ-specific form of disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_assertion evidence source_evidence_literature NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_assertion SIO_000772 14651522 NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_assertion wasDerivedFrom befree-20140225 NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_assertion wasGeneratedBy ECO_0000203 NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP911627.RAFQapKhjvgJmYXP4FZyYoClrMOxKH_FANzK-QAwWGoCM130_provenance.