Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion> ?p ?o ?g. }
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- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion type Assertion NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_head.
- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion evidence source_evidence_literature NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion SIO_000772 11409427 NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion wasDerivedFrom befree-20140225 NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion wasGeneratedBy ECO_0000203 NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.