Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_assertion wasGeneratedBy ECO_0000203 NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_assertion wasDerivedFrom befree-20150227 NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_assertion SIO_000772 21844054 NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_assertion evidence source_evidence_literature NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.
- NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_assertion description "[Dravet syndrome is a rare epileptic encephalopathy linked to mutations in SCN1A (neuronal sodium channel α1 subunit) and characterized by an onset in infancy with polymorphous seizure types and developmental decline.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682522.RAOl5cCXt_RHylB8j-hTMFtrNjrmhy9wNxMVDrPtVZVaE130_provenance.