Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion> ?p ?o ?g. }
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- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion type Assertion NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_head.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion wasGeneratedBy ECO_0000203 NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion wasDerivedFrom befree-20150227 NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion SIO_000772 12470185 NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_assertion evidence source_evidence_literature NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.
- NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_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." NP761444.RAsJYsvo6FW6XzUgbAngeQGGhj-hR9q0mV5omW2O9Z8z8130_provenance.