Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion> ?p ?o ?g. }
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- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion type Assertion NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_head.
- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion wasGeneratedBy ECO_0000203 NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_provenance.
- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion wasDerivedFrom befree-20150227 NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_provenance.
- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion SIO_000772 19191227 NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_provenance.
- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion evidence source_evidence_literature NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_provenance.
- NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_assertion description "[LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817596.RAbPRijUHExaz0WGdPOs9dv6eu3dxwqdD6LGZ-lRjqZoU130_provenance.