@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc> .
@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:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_head {
  this: np:hasAssertion dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion;
    np:hasProvenance dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance;
    np:hasPublicationInfo dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion a np:Assertion .
  
  dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance a np:Provenance .
  
  dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion {
  miriam-gene:1356 a ncit:C16612 .
  
  lld:C0152457 a ncit:C7057 .
  
  dgn-gda:DGNe914ef03f2bcf0d76b3f672e3de01a30 sio:SIO_000628 miriam-gene:1356, lld:C0152457;
    a sio:SIO_001121 .
}

dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_provenance {
  dgn-np:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_assertion dcterms:description
      "[Diagnosis is based on the combination of clinical features and findings such as increased urinary copper excretion, reduced levels of serum ceruloplasmin, high concentrations of copper in liver tissues and Kayser-Fleischer rings.]. 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:17382611;
    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:NP278097.RA7m-IdNI7Uf2RABCViPFVl_95qBEfRvkMpHNhGTf_iGc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}