Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_assertion description "[Taken together, our findings supported a positive association between OPRD1 variants and SD, and a positive haplotypic association between OPRK1 and AD in EAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_assertion evidence source_evidence_literature NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_assertion SIO_000772 17622222 NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_assertion wasDerivedFrom befree-2016 NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_assertion wasGeneratedBy ECO_0000203 NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.
- befree-2016 importedOn "2016-02-19" NP619374.RA1__1vHuBHDTSQ7ybCJVIcZ84fqr8h2xy8l9G-4YLlF0130_provenance.