Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_assertion description "[Complex EGFR mutations are not rare. Gefitinib has different efficacy according to the type of complex EGFR mutations. Patients with Del-19 and L858R mutations may benefit more from gefitinib than other types of complex mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_assertion evidence source_evidence_literature NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_assertion SIO_000772 20808254 NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_assertion wasDerivedFrom gad-20150221 NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_assertion wasGeneratedBy ECO_0000203 NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184887.RAQE5gD13GKCerZVQ8Qa36n5ZdPv3gZRCMoE1SAboLjsU130_provenance.