Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion> ?p ?o ?g. }
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- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion type Assertion NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_head.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion wasGeneratedBy ECO_0000203 NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion wasDerivedFrom befree-2016 NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion SIO_000772 12470185 NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion evidence source_evidence_literature NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.