Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_assertion wasGeneratedBy ECO_0000203 NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_assertion wasDerivedFrom befree-2016 NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_assertion SIO_000772 24439028 NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_assertion evidence source_evidence_literature NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.
- NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_assertion description "[Significant associations were observed with multiple previously identified AMD risk loci and 2 novel genes: HGS (peak SNP rs8070488, MAF = 0.23, OR = 0.91, p = 7.52 × 10(-5)), which plays a role in the clathrin-mediated endocytosis signaling pathway, and TNF (peak SNP rs2071590, MAF = 0.34, OR = 0.89, p = 1.17 × 10(-5)), which is a member of the atherosclerosis signaling and the LXR/RXR activation pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1145990.RAFi9mA93_37ft7kS1qq0Bu_nDjFb9DK4Ips4yGDpdPZA130_provenance.