@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4> .
@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:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_head {
  this: np:hasAssertion dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_assertion;
    np:hasProvenance dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_provenance;
    np:hasPublicationInfo dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_assertion a np:Assertion .
  
  dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_provenance a np:Provenance .
  
  dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_assertion {
  miriam-gene:7001 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGN070ff1af71a0c99076026ac828788c3f sio:SIO_000628 miriam-gene:7001, lld:C0162534;
    a sio:SIO_001121 .
}

dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_provenance {
  dgn-np:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_assertion dcterms:description
      "[There are at least five point mutations and a further five mutations involving five to nine extra repeats of the five octapeptide repeat sequence in the PrP gene, all of which may lead to one of the forms of human prion disease i.e.]. 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:7903647;
    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:NP1325631.RAHcg7m1v1xOYOcnNiSc-uUC0T_RPKmqLptaMEEwMSwp4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:47+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" .
}