Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion> ?p ?o ?g. }
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- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion type Assertion NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_head.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion description "[Mutations in the potassium channel subunit KCNQ2 lead to benign familial neonatal convulsions, a dominantly inherited form of generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion evidence source_evidence_literature NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion SIO_000772 11739564 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion wasDerivedFrom befree-2016 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.
- NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_assertion wasGeneratedBy ECO_0000203 NP338591.RAIan5dwu9TIqXDKBLSsZBcjYSSnkoRvjKodtb5sGJwhY130_provenance.