@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg> .
@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:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_head {
  this: np:hasAssertion dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_assertion;
    np:hasProvenance dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_provenance;
    np:hasPublicationInfo dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_assertion a np:Assertion .
  
  dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_provenance a np:Provenance .
  
  dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0311370 a ncit:C7057 .
  
  dgn-gda:DGN6b26384ceac28860b48c2241ce9aab7b sio:SIO_000628 miriam-gene:7450, lld:C0311370;
    a sio:SIO_001121 .
}

dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_provenance {
  dgn-np:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_assertion dcterms:description
      "[Measurement of von Willebrand factor and intrinsic pathway factors revealed abnormal values in eight patients (low von Willebrand activity in six patients, low factor XII in one patient, and the presence of lupus anticoagulant in one patient).]. 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:8689338;
    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:NP277739.RAcp3zfgojoGpwOYS3QX3k9Z83ZR5bp67EpR60wGljmHg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}