Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_assertion description "[These preliminary results suggest that XPD Lys751Gln and XRCC1 Arg399Gln polymorphisms may not be a significant risk factor for developing CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_assertion evidence source_evidence_literature NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_assertion SIO_000772 18043991 NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_assertion wasDerivedFrom befree-20140225 NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_assertion wasGeneratedBy ECO_0000203 NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540884.RAI_HF9i5yQiXhNa4AYP6_ksLBaPzm7JCPZfcqenHPJ48130_provenance.