Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_assertion description "[This study emphasizes that modifiers such as CD46 and FHL-1 may determine the kidney phenotype of patients who present with homozygous CFH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_assertion evidence source_evidence_literature NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_assertion SIO_000772 23870792 NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_assertion wasDerivedFrom befree-20140225 NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_assertion wasGeneratedBy ECO_0000203 NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690780.RA5wziWTu5oQstGZB0wbtEOyzf2UouUKzlgTb-Ofgptms130_provenance.