Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_assertion description "[A genetic screen was carried out of the open reading frame of SPRN by direct sequencing in 522 patients with prion disease, including 107 with variant Creutzfeldt-Jakob disease (vCJD), and 861 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_assertion evidence source_evidence_literature NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_assertion SIO_000772 18805828 NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_assertion wasDerivedFrom befree-20140225 NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_assertion wasGeneratedBy ECO_0000203 NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869610.RAfjkPdQC_3LJllZO6NDi0EQzv8hC-Qes4uWNnXlmToCA130_provenance.