Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_assertion description "[A common ENTPD1 two-SNP haplotype was associated with increased risk for DM-ESRD (P = 0.0027), and an uncommon four-SNP haplotype was associated with protection against DM-ESRD (P = 0.004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_assertion evidence source_evidence_literature NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_assertion SIO_000772 19095759 NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_assertion wasDerivedFrom befree-20140225 NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_assertion wasGeneratedBy ECO_0000203 NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP617495.RAd8p4C9wbFcFrKg-TClUFomLNXH-_ebHIAYjxxOVtnJ4130_provenance.