Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_assertion description "[Mutations in CACNA1A encoding a neuronal calcium channel and ATP1A2 encoding an ion pump cause episodic ataxia, hemiplegic migraine, and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_assertion evidence source_evidence_literature NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_assertion SIO_000772 16116111 NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_assertion wasDerivedFrom befree-20140225 NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_assertion wasGeneratedBy ECO_0000203 NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811162.RA-bK0AW3MpF7W2nbQFA_vVmad-9KKge-aaAt7T9mQbyQ130_provenance.