Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion> ?p ?o ?g. }
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- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion type Assertion NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_head.
- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion wasGeneratedBy ECO_0000203 NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_provenance.
- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion wasDerivedFrom befree-20140225 NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_provenance.
- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion SIO_000772 15300460 NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_provenance.
- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion evidence source_evidence_literature NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_provenance.
- NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_assertion description "[Ataxia with vitamin E deficiency (AVED) is a rare autosomal recessive neurodegenerative disorder due to mutations in the alpha-tocopherol transfer protein (TTPA) gene on chromosome 8q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225053.RAD4L3C8U7Npqk0UNd4ppyaqGIqyIh6Pv14eOmWGGciMs130_provenance.