@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic> .
@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:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_head {
  this: np:hasAssertion dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_assertion;
    np:hasProvenance dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_provenance;
    np:hasPublicationInfo dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_assertion a np:Assertion .
  
  dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_provenance a np:Provenance .
  
  dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_assertion {
  miriam-gene:5555 a ncit:C16612 .
  
  lld:C1859616 a ncit:C7057 .
  
  dgn-gda:DGNd0cf16b2f09029880edfcf3ecef99243 sio:SIO_000628 miriam-gene:5555, lld:C1859616;
    a sio:SIO_001121 .
}

dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_provenance {
  dgn-np:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_assertion dcterms:description
      "[Whether hereditary protein S, protein C, or antithrombin deficiency is associated with arterial thromboembolism (ATE) and whether history of venous thromboembolism in these subjects predisposes them to subsequent ATE have yet to be determined.]. 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:18824642;
    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:NP928446.RA43AcW6WZsGrPv-MnoG1ZnMaypRAK9v_5Q7ka1vnHcic130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}