Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion> ?p ?o ?g. }
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- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion type Assertion NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_head.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion description "[Two cases with partial deletion of SCN1A and SCN9A and whole SCN1A deletion had an epilepsy phenotype of Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion evidence source_evidence_literature NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion SIO_000772 25524840 NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion wasDerivedFrom befree-2016 NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.
- NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_assertion wasGeneratedBy ECO_0000203 NP1249527.RA-SQsIDoSToyke-7Fn9KuVR7cEcj_Rr5q862UAd4tzjo130_provenance.