Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion evidence source_evidence_literature NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion SIO_000772 16819822 NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion wasDerivedFrom befree-2016 NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_assertion wasGeneratedBy ECO_0000203 NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP558066.RA2hN2LveOt7N9miPiHlm4rCjZTpryaHym_SJaEcSUO3Y130_provenance.