Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_assertion description "[Recently, two novel sequence differences in the B1R gene were identified, and the C allele of the G-->C substitution at position -699 in the promoter region of the B1R gene was found to be less frequent among patients with ESRD compared with healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_assertion evidence source_evidence_literature NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_assertion SIO_000772 10505688 NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_assertion wasDerivedFrom befree-20140225 NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_assertion wasGeneratedBy ECO_0000203 NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860639.RAbGifB0J91WtGvyjD1kyz3qJ1jyUVQ3RyyKUzNgBtuIk130_provenance.