@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA> .
@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:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_head {
  this: np:hasAssertion dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_assertion;
    np:hasProvenance dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_provenance;
    np:hasPublicationInfo dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_assertion a np:Assertion .
  
  dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_provenance a np:Provenance .
  
  dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_assertion {
  miriam-gene:1123 a ncit:C16612 .
  
  lld:C0013261 a ncit:C7057 .
  
  dgn-gda:DGNfeab0e6831f7f8a39b57ed6d750b2e15 sio:SIO_000628 miriam-gene:1123, lld:C0013261;
    a sio:SIO_001122 .
}

dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_provenance {
  dgn-np:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_assertion dcterms:description
      "[DRS (Duane retraction syndrome) linked to the DURS2 locus is associated with bilateral abnormalities of many orbital motor nerves, and structural abnormalities of all EOMs except those innervated by the inferior division of CN3.]. 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:17197533;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP152793.RACGqjzHmDAjOUzQXCEHDnu6pVNHdOLNZKpVGFB-qijVA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:21+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" .
}