@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM> .
@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:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_head {
  this: np:hasAssertion dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_assertion;
    np:hasProvenance dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_provenance;
    np:hasPublicationInfo dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_assertion a np:Assertion .
  
  dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_provenance a np:Provenance .
  
  dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0022116 a ncit:C7057 .
  
  dgn-gda:DGN393b902d21c17503477f13dc3874008c sio:SIO_000628 miriam-gene:7157, lld:C0022116;
    a sio:SIO_001121 .
}

dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_provenance {
  dgn-np:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_assertion dcterms:description
      "[The aim of our investigation was to study the connection between p53 gene Bam HI RFLP polymorphism and the brain infarction volume in patients with atherothrombotic ischemic stroke that could highlight certain genetic aspects of the individual sensibility of brain tissue to acute ischemia.]. 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:15272143;
    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:NP875479.RAM1WfIU-4xRJw-0IMau1o2rsUO45bWJvg83jXsTWO3fM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}