Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_assertion description "[Are the T/C polymorphism of the CYP17 gene and the tetranucleotide repeat (TTTA) polymorphism of the CYP19 gene genetic markers for premature coronary artery disease in Caucasians?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_assertion evidence source_evidence_literature NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_assertion SIO_000772 16045239 NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_assertion wasDerivedFrom befree-20150227 NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_assertion wasGeneratedBy ECO_0000203 NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP344508.RA888_7EBJKm2Xln7hIHVCbV98VzzNDZpwe4B2RQL-NEA130_provenance.