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- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion type Assertion NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_head.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion wasGeneratedBy ECO_0000203 NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion wasDerivedFrom befree-20150227 NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion SIO_000772 12470185 NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_assertion evidence source_evidence_literature NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.
- NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_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." NP761478.RAs4Ehq-kKw0aZlw-3tWIcMR5yVlr_uw0pg7quGvjy_vg130_provenance.