Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion> ?p ?o ?g. }
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- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion type Assertion NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_head.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_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." NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion evidence source_evidence_literature NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion SIO_000772 16819822 NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion wasDerivedFrom befree-20140225 NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_assertion wasGeneratedBy ECO_0000203 NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.