Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_assertion description "[Analysis of the association of studied MTHFR C677T, A1298C and ACE I/D polymorphisms with albuminuria showed that the MTHFR 677 T polymorphism, in the recessive and dominant models, was a risk factor for both micro and macroalbuminuria, while the ACE DD mutant genotype was a risk factor for microalbuminuria and the MTHFR 1298C in the dominant model only was a risk factor for macroalbuminuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_assertion evidence source_evidence_literature NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_assertion SIO_000772 22554825 NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_assertion wasDerivedFrom befree-20140225 NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_assertion wasGeneratedBy ECO_0000203 NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211738.RA5XjBIHCzxUfwncErI8G7nkAG1tDQFawA3b4-QfKAjYc130_provenance.