Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion> ?p ?o ?g. }
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- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion type Assertion NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_head.
- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion description "[Knowledge of an expanded spectrum of epileptic encephalopathies associated with SCN1A mutations allows earlier diagnostic confirmation for children with these devastating disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_provenance.
- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion evidence source_evidence_literature NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_provenance.
- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion SIO_000772 17347258 NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_provenance.
- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion wasDerivedFrom befree-2016 NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_provenance.
- NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_assertion wasGeneratedBy ECO_0000203 NP597933.RAeowkrzXiKo4Mz8m0ryoNefOm-ZtIx6GVpvgxCJ6PcVA130_provenance.