@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w> .
@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:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_head {
  this: np:hasAssertion dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_assertion;
    np:hasProvenance dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_provenance;
    np:hasPublicationInfo dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_assertion a np:Assertion .
  
  dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_provenance a np:Provenance .
  
  dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0040038 a ncit:C7057 .
  
  dgn-gda:DGN2735aa9b81d6ecc9138bd15b8db93c55 sio:SIO_000628 miriam-gene:324, lld:C0040038;
    a sio:SIO_001121 .
}

dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_provenance {
  dgn-np:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_assertion dcterms:description
      "[These data indicate that individuals carrying the 4600AG genotype have high sEPCR levels but do not have an increased risk of thrombosis, whereas individuals carrying the 4678CC genotype have higher APC levels and lower risk of venous thromboembolism.]. 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:15116250;
    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:NP660147.RAAiOvxuNqET9Zhf8lHsNiRcefzak4eMoQBk49usc4j2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}