Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_assertion description "[Interestingly, all marginally significant SNPs in SLC19A1 are in strong linkage disequilibrium (r(2)> or = 0.8) with the nonsynonymous coding SNP rs1051266 (c.80A>G), which has previously been associated with nonsyndromic cases of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_assertion evidence source_evidence_literature NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_assertion SIO_000772 20718043 NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_assertion wasDerivedFrom befree-20140225 NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_assertion wasGeneratedBy ECO_0000203 NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP225230.RA4Hq0uDd8GU7m52bKf_73gaM8n4z3FV-tMjuLj0RSFMA130_provenance.