Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion> ?p ?o ?g. }
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- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion type Assertion NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_head.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion wasGeneratedBy ECO_0000203 NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion wasDerivedFrom befree-20140225 NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion SIO_000772 12470185 NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_assertion evidence source_evidence_literature NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.
- NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_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." NP581107.RArLGEkE1NCyjVLkCmh4LWPJzN89YG1yrhgaupdkbvqlw130_provenance.