Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.