Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion description "[Episodic ataxia type 1 (EA1) is caused by mutations in the KCNA1 gene encoding the fast potassium channel Kv1.1 and is characterized clinically by brief episodes of ataxia and continuous and spontaneous motor unit activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion evidence source_evidence_literature NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion SIO_000772 23909822 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion wasDerivedFrom befree-20150227 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_assertion wasGeneratedBy ECO_0000203 NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521267.RAYJBxn2EJifITB7hJnGGKNUoYjxGcqjNLqiqS-3ps6xE130_provenance.