Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_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." NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_assertion evidence source_evidence_literature NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_assertion SIO_000772 2685311 NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_assertion wasDerivedFrom befree-20140225 NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_assertion wasGeneratedBy ECO_0000203 NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP328694.RAJDy-Ka8GnibsFtYRrpeAkFqjrcPCgoY3MnB3I79lKQ0130_provenance.