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- source_evidence_literature type ECO_0000212 NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_assertion description "[This figure is comparable to the percentage of RP2 gene mutations that we have detected in our entire XLRP patient pool (10%-15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_assertion evidence source_evidence_literature NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_assertion SIO_000772 10480356 NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_assertion wasDerivedFrom befree-20150227 NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_assertion wasGeneratedBy ECO_0000203 NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674448.RAHlaz39q8IN1eHSaMi5g_Kn_klOXMQd8xV7wOY62e0i0130_provenance.