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- source_evidence_literature type ECO_0000212 NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_assertion description "[In a hospital-based, case-control study of 830 non-Hispanic white patients with SCCHN and 854 cancer-free, matched control participants, the authors genotyped the ADPRT alanine 762 valine (Ala762Val) single-nucleotide polymorphism (SNP), the XRCC1 arginine 399 glutamine (Arg399Gln) SNP, and the APE aspartic acid 148 glutamic acid (Asp148Glu) SNP and assessed their associations with the risk of SCCHN in multivariate logistic regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_assertion evidence source_evidence_literature NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_assertion SIO_000772 17614107 NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_assertion wasDerivedFrom befree-20140225 NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_assertion wasGeneratedBy ECO_0000203 NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP413450.RAl-fFxr0u5-_hCZosSNLhgdJdCFyMRcXeSEi-KHm4lP8130_provenance.