Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- befree-2016 importedOn "2016-02-19" NP376879.RADcIKHIFD2Xww1s_nUdmEqI6fSyzA2TtuLtTK_UWUpkE130_provenance.
- 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.