@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME> .
@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:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_head {
  this: np:hasAssertion dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion;
    np:hasProvenance dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance;
    np:hasPublicationInfo dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion a np:Assertion .
  
  dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance a np:Provenance .
  
  dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion {
  miriam-gene:4072 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN3676b18c57de51f8c32762b3b0ccdc18 sio:SIO_000628 miriam-gene:4072, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_provenance {
  dgn-np:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_assertion dcterms:description
      "[Further larger studies are needed to (1) estimate the prevalence of this mutant among individuals belonging to different KSA locations (2) assess the relative contribution of this mutational event separately and in combination with other thrombophilic polymorphisms in the etiology of cardiovascular disease in KSA.]. 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:21553052;
    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:NP361299.RAQlWCimAy5g7ws8QIWebGn6s5PPFUsrtJ-KO_czXVFME130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:31+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" .
}