Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion> ?p ?o ?g. }
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- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion type Assertion NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_head.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion description "[Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion evidence source_evidence_literature NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion SIO_000772 25524840 NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion wasDerivedFrom befree-2016 NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.
- NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_assertion wasGeneratedBy ECO_0000203 NP1249535.RAs0rmC6WIvnzvemIci_DHOPfyn1K3YEdOpCsfdANi59c130_provenance.