Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion description "[Ataxia with vitamin E deficiency (AVED), or familial isolated vitamin E deficiency, is a rare autosomal recessive neurodegenerative disease characterized clinically by symptoms with often striking resemblance to those of Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion evidence source_evidence_literature NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion SIO_000772 9463307 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion wasDerivedFrom befree-20150227 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_assertion wasGeneratedBy ECO_0000203 NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP411517.RAJVh3Fs5zB4ajTdhJ9AKmpH5DRc0FdBQuipy0yu1n9rE130_provenance.