Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_assertion wasGeneratedBy ECO_0000203 NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_assertion wasDerivedFrom befree-20140225 NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_assertion SIO_000772 1674696 NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_assertion evidence source_evidence_literature NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_assertion description "[A number of mutations have been demonstrated in the open reading frame (ORF) of the prion protein (PrP) gene in patients with familial Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP725023.RADtj0S2JwRuOq6aVCnN0Hdq3jdzrGJkX22_HFRrWIJYg130_provenance.