@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14> .
@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/v3.0.0/void/> .

dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_head {
  this: np:hasAssertion dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion;
    np:hasProvenance dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance;
    np:hasPublicationInfo dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion a np:Assertion .
  
  dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance a np:Provenance .
  
  dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion {
  miriam-gene:538 a ncit:C16612 .
  
  lld:C0268070 a ncit:C7057 .
  
  dgn-gda:DGNd0feb8a4c4c666469c13a8df53870a97 sio:SIO_000628 miriam-gene:538, lld:C0268070;
    a sio:SIO_001121 .
}

dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_provenance {
  dgn-np:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_assertion dcterms:description
      "[In more than 40 years since copper deficiency was delineated in pediatric subjects with Menkes disease, remarkable advances in our understanding of the clinical, biochemical, and molecular aspects of the human copper transporter ATP7A have emerged.]. 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:24735419;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP257131.RA4o7DhJDFtW0My07gZ430T1CdJYTLk2EAP_3o5lyyg14130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:06+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}