Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_assertion wasGeneratedBy ECO_0000203 NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_assertion wasDerivedFrom befree-20150227 NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_assertion SIO_000772 22606975 NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_assertion evidence source_evidence_literature NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.
- NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_assertion description "[Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP976593.RA0CU766cukkFtMmKmRwE9E9VIsRtRmSVsIr7BcSma81U130_provenance.