Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_assertion description "[In addition, the results of combined genotype analysis of these two SNPs showed a borderline significant association between CYP3A4 and VDR TaqI combined variant genotypes and PRCa risk (RR=3.43; 95% CI=0.99-11.77).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_assertion evidence source_evidence_literature NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_assertion SIO_000772 12644831 NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_assertion wasDerivedFrom befree-20140225 NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_assertion wasGeneratedBy ECO_0000203 NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP349452.RABHgyHDC-qkAkdg0r0oktqFT0QtYYMDTUEexaUl4afA4130_provenance.