Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_assertion description "[Deletion of two closely related genes, complement factor H-related 1 (CFHR1) and complement factor H-related 3 (CFHR3), increases the risk of atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_assertion evidence source_evidence_literature NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_assertion SIO_000772 17367211 NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_assertion wasDerivedFrom lhgdn-20090331 NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_assertion wasGeneratedBy ECO_0000203 NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212107.RABdVxkEt12SmMmATMB6ZyMdMxEz1KO-MHE_3TYpN6cb4130_provenance.