Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion> ?p ?o ?g. }
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- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion type Assertion NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_head.
- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion description "[A patient with episodic ataxia, seizures, migraine, and alternating hemiplegia has a heterozygous mutation in SLC1A3 that is not present in his asymptomatic parents and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_provenance.
- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion evidence source_evidence_literature NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_provenance.
- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion SIO_000772 16116111 NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_provenance.
- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion wasDerivedFrom befree-2016 NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_provenance.
- NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_assertion wasGeneratedBy ECO_0000203 NP510176.RAV5NHWjn8vDSXaFy1ZvtUmUSta5XNV8gwZF4QhPvO9rk130_provenance.