Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion> ?p ?o ?g. }
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- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion type Assertion NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_head.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_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." NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion evidence source_evidence_literature NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion SIO_000772 16116111 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion wasDerivedFrom befree-20140225 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.
- NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_assertion wasGeneratedBy ECO_0000203 NP678979.RAmrn3AYUDIlwHKwJogvXV2M-2WzuCnSRTteakHpedhNU130_provenance.