Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_assertion description "[Although case-control studies suggest that African Americans with common coding variants in the APOL1 gene are 5-29 times more likely than those individuals without such variants to have focal segmental glomerulosclerosis, HIV-associated nephropathy, or ESRD, prospective studies have not yet evaluated the impact of these variants on CKD in a community-based sample of African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_assertion evidence source_evidence_literature NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_assertion SIO_000772 23766536 NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_assertion wasDerivedFrom befree-2016 NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_assertion wasGeneratedBy ECO_0000203 NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1086001.RAdSZW-4A-s9eYa47jPwJjWdAJAiYenMywLbISEeHe_vg130_provenance.