@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI> .
@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 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:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_head {
  this: np:hasAssertion dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion;
    np:hasProvenance dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance;
    np:hasPublicationInfo dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion a np:Assertion .
  
  dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance a np:Provenance .
  
  dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion {
  miriam-gene:2155 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNb5b29fcbc6d881dd215ed98462970f4f sio:SIO_000628 miriam-gene:2155, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_provenance {
  dgn-np:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_assertion dct:description
      "[This study shows that for some genes, further studies are unnecessary, whereas for others, no more enrollments are needed. The impact of certain genotypes must be examined in relation to other established risk factors and potentially new therapeutic strategies.]. 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:11397354;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP44335.RApFQ_umxE5pZOHM1T-d9OuY8zCEmHZHd7uAY39UQl4rI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}