@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik> .
@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:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_head {
  this: np:hasAssertion dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion;
    np:hasProvenance dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance;
    np:hasPublicationInfo dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion a np:Assertion .
  
  dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance a np:Provenance .
  
  dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGN1ccfa2b103a6004db2c2d985ff64e041 sio:SIO_000628 miriam-gene:5621, lld:C0162534;
    a sio:SIO_001121 .
}

dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance {
  dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion dcterms:description
      "[The main cause for the development of transmissible spongiform encephalopathies (TSE) is the conformational change of prion protein from the normal cellular isoform (PrP(C)) into the abnormal isoform, named prion (PrP(Sc)).]. 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:17884181;
    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:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:31+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" .
}