Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_assertion description "[Real-time PCR-based genotyping method developed here is useful for investigations of allelic asymmetries within genomic regions with variations found in retinitis pigmentosa and retinl degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_assertion evidence source_evidence_literature NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_assertion SIO_000772 18450588 NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_assertion wasDerivedFrom lhgdn-20090331 NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_assertion wasGeneratedBy ECO_0000203 NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP185514.RA5u39RGDcSeWCPFcEI-evwkVda4yV6Q19fjZCoY_uM_A130_provenance.