Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_assertion description "[The coding region of NPY2R was analysed for mutations in 48 obese Danish white subjects and two silent substitutions were identified: SNPs 1 and 2 (rs1047214 and rs2880415).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_assertion evidence source_evidence_literature NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_assertion SIO_000772 17019604 NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_assertion wasDerivedFrom befree-20140225 NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_assertion wasGeneratedBy ECO_0000203 NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487190.RAd04LuKfa3vRZ8q1Ko8c_BUmMYXPHF8s_Zi_NW7LGtqM130_provenance.