@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM> .
@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:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_head {
  this: np:hasAssertion dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion;
    np:hasProvenance dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance;
    np:hasPublicationInfo dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion a np:Assertion .
  
  dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance a np:Provenance .
  
  dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0751956 a ncit:C7057 .
  
  dgn-gda:DGN3b4f0d62002aae095aefabbff8d8b675 sio:SIO_000628 miriam-gene:472, lld:C0751956;
    a sio:SIO_001121 .
}

dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_provenance {
  dgn-np:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_assertion dcterms:description
      "[This study was performed in acute stroke patients in the Turkish population to determine the frequency of the A1166C polymorphism in the AT1 gene and to examine the role of this polymorphism in acute stroke development.]. 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:23480670;
    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:NP240332.RAM-Wf15UrAsii7SrraEz7LphMi3yvC43Schiv-8otRBM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}