Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_assertion description "[In this study, four new K12 mutations (Arg135Gly, Arg135Ile, Tyr429Asp, and Leu140Arg) were identified in three unrelated MCD pedigrees and in one individual with MCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_assertion evidence source_evidence_literature NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_assertion SIO_000772 9399908 NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_assertion wasDerivedFrom befree-20150227 NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_assertion wasGeneratedBy ECO_0000203 NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529036.RAbaPB3Zg2X5dDUyorTV7yeX80Xq0bymsj-7WGZF9iYH8130_provenance.