Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_assertion description "[In this study, NR2E3 mutations (p.G56R, p.V118M) were found to be responsible for approximately 2.9% of overall RP in Chinese patients, comparable to the contributions of RHO and RP1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_assertion evidence source_evidence_literature NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_assertion SIO_000772 19933183 NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_assertion wasDerivedFrom befree-20140225 NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_assertion wasGeneratedBy ECO_0000203 NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP726550.RAmgKlnL1eKSreUMET2ZEMKwQr9lmqf5zUKrFXd8owT_k130_provenance.