@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw> .
@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:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_head {
  this: np:hasAssertion dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion;
    np:hasProvenance dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance;
    np:hasPublicationInfo dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion a np:Assertion .
  
  dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance a np:Provenance .
  
  dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  
  lld:C0272375 a ncit:C7057 .
  
  dgn-gda:DGN8c4b8a7123aa4f9ac7b762f9873a4d6c sio:SIO_000628 miriam-gene:5660, lld:C0272375;
    a sio:SIO_001121 .
}

dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance {
  dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion dcterms:description
      "[In addition, inherited prothrombotic defects, such as protein C, protein S, and antithrombin deficiencies, and genetic mutations for FV Leiden, prothrombin gene G20210A (FII G20210A), and methyltetrahydrofolate reductase C677T (MTHFR C677T) were studied.]. 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:22048515;
    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:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:59+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" .
}