Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_assertion description "[We conclude that array CGH be considered an important investigation in adults with complicated epilepsy and, at least at present for selected patients, should join the diagnostic repertoire of clinical history and examination, neuroimaging, electroencephalography and other indicated investigations in generating a more complete formulation of an individual's epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_assertion evidence source_evidence_literature NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_assertion SIO_000772 22342432 NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_assertion wasDerivedFrom befree-20150227 NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_assertion wasGeneratedBy ECO_0000203 NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470220.RAV42fpIxxGsi8QBGZsuZm7pxp3yLBPdEwolTzb4LLEso130_provenance.