Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion> ?p ?o ?g. }
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- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion type Assertion NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_head.
- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion description "[Gene mutations associated with epilepsy are known, to date, only for two disorders: the lissencephaly 1 gene in Miller-Dieker syndrome and mutations in the UBE3A gene in Angelman syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_provenance.
- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion evidence source_evidence_literature NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_provenance.
- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion SIO_000772 11579431 NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_provenance.
- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion wasDerivedFrom befree-2016 NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_provenance.
- NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_assertion wasGeneratedBy ECO_0000203 NP331485.RA0vdHAx_RCu9iQ9XNMvNJoxWCp1pHHOS5rhzUz2YKFsM130_provenance.