@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs> .
@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:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_head {
  this: np:hasAssertion dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_assertion;
    np:hasProvenance dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_provenance;
    np:hasPublicationInfo dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_assertion a np:Assertion .
  
  dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_provenance a np:Provenance .
  
  dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_assertion {
  miriam-gene:2157 a ncit:C16612 .
  
  lld:C0042974 a ncit:C7057 .
  
  dgn-gda:DGN8f2d8d5bfe5d9a3b2aebea91ad944cba sio:SIO_000628 miriam-gene:2157, lld:C0042974;
    a sio:SIO_001121 .
}

dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_provenance {
  dgn-np:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_assertion dcterms:description
      "[Considering the recent suggestion that platelet membrane glycoprotein polymorphisms (PltGPs) may play a role as modulators of thromboembolic or haemorrhagic diseases, we investigated the role of different PltGPs and GPVI content in the clinical expression of patients with VWD type 1.The diagnosis of VWD (n = 76) was based on laboratory findings (VWF:Ag, VWF:RCo, VWF:CB, FVIII:C, and multimer analysis), family and personal history of bleeding.]. 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:14652648;
    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:NP178571.RAOXFlHu3YY40N4FgdHvSb_RtASvzQpZoLYCXjEtFKRAs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}