Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP400654.RA1fMPlwL6FCy1nG555GTBhymmSvcFwei9lr8y0byij8A130_provenance.