@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg> .
@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:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_head {
  this: np:hasAssertion dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_assertion;
    np:hasProvenance dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_provenance;
    np:hasPublicationInfo dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_assertion a np:Assertion .
  
  dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_provenance a np:Provenance .
  
  dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_assertion {
  miriam-gene:324 a ncit:C16612 .
  
  lld:C0040038 a ncit:C7057 .
  
  dgn-gda:DGN3f06f538d4c59fcc69154444d01b0c36 sio:SIO_000628 miriam-gene:324, lld:C0040038;
    a sio:SIO_001121 .
}

dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_provenance {
  dgn-np:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_assertion dcterms:description
      "[Here we have analysed 125 consecutive patients with incidental or recurrent venous thromboembolism for the presence of mutations at the cleavage sites for APC at amino acid positions Arg336 and Arg562 of factor VIII.]. 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:8616046;
    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:NP656333.RAtqBCx3xHrd10ST14KjuatInQU2X2tAg3TqCZowKVdLg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}