@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_head {
  this: np:hasAssertion dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_assertion;
    np:hasProvenance dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_provenance;
    np:hasPublicationInfo dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_assertion a np:Assertion .
  
  dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_provenance a np:Provenance .
  
  dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0751254 a ncit:C7057 .
  
  dgn-gda:DGN72d5a9c934d2dd6f7ca01513be0e50ee sio:SIO_000628 miriam-gene:5621, lld:C0751254;
    a sio:SIO_001121 .
}

dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_provenance {
  dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_assertion dcterms:description
      "[Nonsynonymous mutations in the human prion protein (HuPrP) gene contribute to the conversion of HuPrP(C) to HuPrP(Sc) and amyloid formation which in turn leads to prion diseases such as familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:23527686;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP1063382.RAaMemNjGo2xoexMn_dOcgHFBMeBkTRHOkt-FpU2CCG0w130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:48+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}