Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_assertion description "[A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_assertion evidence source_evidence_literature NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_assertion SIO_000772 17668384 NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_assertion wasDerivedFrom befree-2016 NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_assertion wasGeneratedBy ECO_0000203 NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.
- befree-2016 importedOn "2016-02-19" NP622869.RAe6y52i9PZC-XS4ZplNtfHqr6S4yTLTOr1LcueclQ9LY130_provenance.