Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- befree-2016 importedOn "2016-02-19" NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_assertion wasGeneratedBy ECO_0000203 NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_assertion wasDerivedFrom befree-2016 NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_assertion SIO_000772 19204046 NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_assertion evidence source_evidence_literature NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.
- NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_assertion description "[A gain-of-function (E/D) mutation in the pore-forming alpha subunit (Slo1) of the BK channel was recently identified and is linked to human neurological diseases of coexistent generalized epilepsy and paroxysmal dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719457.RAXfP9-fQzgRm_SFLKAE7kulgi5Z0gHSUxmd-wPZA50zU130_provenance.