@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_head {
  this: np:hasAssertion dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_assertion;
    np:hasProvenance dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_provenance;
    np:hasPublicationInfo dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_assertion a np:Assertion .
  
  dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_provenance a np:Provenance .
  
  dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_assertion {
  miriam-gene:241 a ncit:C16612 .
  
  lld:C0007786 a ncit:C7057 .
  
  dgn-gda:DGN812bd68020b422c4d353e7d53cdac3c9 sio:SIO_000628 miriam-gene:241, lld:C0007786;
    a sio:SIO_001122 .
}

dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_provenance {
  dgn-np:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_assertion dcterms:description
      "[The ALOX5AP SG13S114 variant is an independent risk factor for IS in the Iberian population and is associated with ALOX5AP expression levels. The role of this gene in stroke merits further investigation.]. 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:20357438;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP106119.RAV89FYx_4AGDeYZhVdSMbzGNxErbpSH6RAfWg5Pyez8k130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:38+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}