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- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion type Assertion NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_head.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion wasGeneratedBy ECO_0000203 NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion wasDerivedFrom befree-2016 NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion SIO_000772 12470185 NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_assertion evidence source_evidence_literature NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.
- NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_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." NP376878.RABTxw6VoSd3H3H89xWWQsptKFQB681-NsO-IBm_t2v2o130_provenance.