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- source_evidence_literature type ECO_0000212 NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- befree-2016 importedOn "2016-02-19" NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_assertion wasGeneratedBy ECO_0000203 NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_assertion wasDerivedFrom befree-2016 NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_assertion SIO_000772 11803489 NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_assertion evidence source_evidence_literature NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.
- NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_assertion description "[No statistically significant association was observed between sequence variants in the ELOVL(4) gene and susceptibility to AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342661.RA4RwKSx8pW-N2e7NezWtLJbJ1cNoHchMNWta_2c6KghM130_provenance.