@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_head {
  this: np:hasAssertion dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_assertion;
    np:hasProvenance dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_provenance;
    np:hasPublicationInfo dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_assertion a np:Assertion .
  
  dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_provenance a np:Provenance .
  
  dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0019202 a ncit:C7057 .
  
  dgn-gda:DGN3ddc0f9306790e8db91900579f934923 sio:SIO_000628 miriam-gene:348, lld:C0019202;
    a sio:SIO_001121 .
}

dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_provenance {
  dgn-np:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_assertion dcterms:description
      "[The APOE genotypes (APOE ε3/ε3 (wild-type), APOE ε2-positive, and APOE ε4-positive) were determined and the APOE genotype effect on the phenotypic WD presentation was assessed in all symptomatic WD patients, as well as in patient subgroups divided according to sex and ATP7B genotype.]. 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:22221592;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP247947.RAZUhDqA2BbUJ8MhAKhQycYKHmsm10Qqvp7KRstcubDeY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}