Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion> ?p ?o ?g. }
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- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion type Assertion NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_head.
- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion description "[They include well-recognized syndromes such as tuberous sclerosis complex, epilepsy associated with Rett syndrome, some of the progressive myoclonic epilepsies, and novel disorders such as epilepsy associated with mutations in the PCDH 19 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_provenance.
- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion evidence source_evidence_literature NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_provenance.
- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion SIO_000772 22946725 NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_provenance.
- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion wasDerivedFrom befree-2016 NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_provenance.
- NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_assertion wasGeneratedBy ECO_0000203 NP1010132.RAWfKaE_XLK7VnX6yrbjlDJLzSr3s7zbycqPcVDLUJLxs130_provenance.