@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE> .
@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:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_head {
  this: np:hasAssertion dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion;
    np:hasProvenance dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance;
    np:hasPublicationInfo dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion a np:Assertion .
  
  dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance a np:Provenance .
  
  dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion {
  miriam-gene:302 a ncit:C16612 .
  
  lld:C0029445 a ncit:C7057 .
  
  dgn-gda:DGN0270070fd20e125e5350cb266d0f1ad9 sio:SIO_000628 miriam-gene:302, lld:C0029445;
    a sio:SIO_001122 .
}

dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance {
  dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion dct:description
      "[These genes are important in bone morphology, metabolism and vascular disease. Our results may provide insight into the pathogenesis of osteonecrosis in sickle cell disease, help identify individuals who are at high risk for osteonecrosis, and thus allow earlier and more effective therapeutic intervention.]. 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:15784727;
    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:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+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" .
}