@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM> .
@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:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_head {
  this: np:hasAssertion dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_assertion;
    np:hasProvenance dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_provenance;
    np:hasPublicationInfo dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_assertion a np:Assertion .
  
  dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_provenance a np:Provenance .
  
  dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_assertion {
  miriam-gene:538 a ncit:C16612 .
  
  lld:C0267244 a ncit:C7057 .
  
  dgn-gda:DGN418545e20a7f75f9a56d3c2674f8af1f sio:SIO_000628 miriam-gene:538, lld:C0267244;
    a sio:SIO_001121 .
}

dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_provenance {
  dgn-np:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_assertion dcterms:description
      "[The majority of genes identified by RDA showed nearly complete concordance with microarray results, and also led to the identification of some differentially expressed genes such as lysyl oxidase, copper transporter ATP7A, EphB6, RUNX2 and a variant of RUNX2.]. 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:16314837;
    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:NP315518.RAfweZ98G7eoAFNeV3OXdVfMHBSoIyIDB2Iih8yU6i3rM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}