@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU> .
@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:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_head {
  this: np:hasAssertion dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_assertion;
    np:hasProvenance dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_provenance;
    np:hasPublicationInfo dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_assertion a np:Assertion .
  
  dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_provenance a np:Provenance .
  
  dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_assertion {
  miriam-gene:142 a ncit:C16612 .
  
  lld:C0007785 a ncit:C7057 .
  
  dgn-gda:DGN7c0c2e9df833e8ce15db4d85932d3404 sio:SIO_000628 miriam-gene:142, lld:C0007785;
    a sio:SIO_001121 .
}

dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_provenance {
  dgn-np:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_assertion dcterms:description
      "[Our data thus suggest that the tested PARP polymorphisms do not principally contribute to cerebral infarction, although extensive searches would be required to clarify whether the PARP gene plays an important role in the pathogenesis of human stroke.]. 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:10657571;
    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:NP519978.RAdFveXyl-ugrs9fsCaa8hlziZbKfk7Tc8sR2UIYIGFTU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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" .
}