Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_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." NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_assertion evidence source_evidence_literature NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_assertion SIO_000772 2685311 NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_assertion wasDerivedFrom befree-20150227 NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_assertion wasGeneratedBy ECO_0000203 NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647554.RAFUnBpiegDjj7rXklQqCJ5wafGCPHjktCeQ1t4QCTIl0130_provenance.