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- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion type Assertion NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_head.
- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion wasGeneratedBy ECO_0000203 NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.
- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion wasDerivedFrom befree-20140225 NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.
- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion SIO_000772 19220312 NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.
- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion evidence source_evidence_literature NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.
- NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_assertion description "[Here, we identified a novel SCN1A L263V mutation in a Portuguese family with partly co-segregating hemiplegic migraine and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506784.RAJT5Glou5dEYUerkZeOw6Q6HreK91D_vajpRZ5JChct4130_provenance.