Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_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." NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_assertion evidence source_evidence_literature NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_assertion SIO_000772 23870792 NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_assertion wasDerivedFrom befree-20150227 NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_assertion wasGeneratedBy ECO_0000203 NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP549788.RANkRb6RG4rvh9lvUJG4CHAAtPK1BUCCgSC7-B7m6tTD8130_provenance.