@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14> .
@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:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_head {
  this: np:hasAssertion dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_assertion;
    np:hasProvenance dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_provenance;
    np:hasPublicationInfo dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_assertion a np:Assertion .
  
  dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_provenance a np:Provenance .
  
  dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  
  lld:C0018799 a ncit:C7057 .
  
  dgn-gda:DGN4281a2aa512758d6f49933181be88e5f sio:SIO_000628 miriam-gene:5660, lld:C0018799;
    a sio:SIO_001121 .
}

dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_provenance {
  dgn-np:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_assertion dcterms:description
      "[They include cardiac disease, vascular abnormalities, endothelial damage, infectious diseases, collagen tissue diseases, certain inborn errors of metabolism and anticardiolipin antibody, lupus anticoagulant and deficiencies of protein C, protein S, antithrombin or plasminogen.]. 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:19432826;
    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:NP419897.RABnCYRngsG_jbF030rc0V1yUDSURk_8qNOgtiEsSeA14130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}