@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco> .
@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:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_head {
  this: np:hasAssertion dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion;
    np:hasProvenance dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance;
    np:hasPublicationInfo dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion a np:Assertion .
  
  dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance a np:Provenance .
  
  dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0022336 a ncit:C7057 .
  
  dgn-gda:DGN4a3274fb52e42df30f129c61c3aeb742 sio:SIO_000628 miriam-gene:5621, lld:C0022336;
    a sio:SIO_001121 .
}

dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance {
  dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion dcterms:description
      "[Familial CJD accounts for approximately 10% of all European cases of CJD, and is associated with inherited mutations of the prion protein gene, caused by one of the 24 single amino acid substitutions or insertions of octapeptide repeats.]. 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:12064251;
    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:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:27+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" .
}