Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_assertion wasGeneratedBy ECO_0000218 NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_assertion wasDerivedFrom ctd_human-20130708 NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_assertion SIO_000772 12470185 NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_assertion evidence source_evidence_curated NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_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." NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP33095.RAiZBvgiAQYulGPWG-2GSjWk5YL60BCFUeoG9uELm3Q54130_provenance.