@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_head {
  this: np:hasAssertion dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_assertion;
    np:hasProvenance dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_provenance;
    np:hasPublicationInfo dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_assertion a np:Assertion .
  
  dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_provenance a np:Provenance .
  
  dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_assertion {
  miriam-gene:22915 a ncit:C16612 .
  
  lld:C0005818 a ncit:C7057 .
  
  dgn-gda:DGN26fbadde7f321511194990a0a7dd8d5b sio:SIO_000628 miriam-gene:22915, lld:C0005818;
    a sio:SIO_001121 .
}

dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_provenance {
  dgn-np:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_assertion dcterms:description
      "[These data indicate that patients with factor V Quebec have an inherited bleeding disorder distinct from other platelet disorders and associated with multiple abnormalities, including multimerin deficiency, abnormal platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen, and an epinephrine aggregation defect.]. 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:8652809;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1351299.RAkj69xU61I2nLcd4WRL4e018vRIx4cmpmACzKYCn4Prk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:58+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}