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- source_evidence_literature type ECO_0000212 NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_assertion description "[We also postulate that the patient's disorder, reminiscent of a spongy glioneuronal dystrophy as seen in Alper's and Creutzfeldt-Jakob diseases, may be secondary to the presence of the pathogenic isoform of the prion protein encoded by a gene mapped to 20p12----pter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_assertion evidence source_evidence_literature NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_assertion SIO_000772 2685311 NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_assertion wasDerivedFrom befree-2016 NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_assertion wasGeneratedBy ECO_0000203 NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296092.RAxUad2s8erWc6Up8GPYWbUECdThsPPkofBbcyrk5LoUo130_provenance.