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- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion type Assertion NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_head.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion evidence source_evidence_literature NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion SIO_000772 23429546 NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion wasDerivedFrom befree-2016 NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.
- NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_assertion wasGeneratedBy ECO_0000203 NP1054803.RAG1zh5A4V0koxC6Zdh6SvjwK7I1sJYoSpQD8GJIw3wBA130_provenance.