@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0> .
@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 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:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_head {
  this: np:hasAssertion dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion;
    np:hasProvenance dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance;
    np:hasPublicationInfo dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion a np:Assertion .
  
  dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance a np:Provenance .
  
  dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  
  lld:C1282975 a ncit:C7057 .
  
  dgn-gda:DGN45720a0675594c9c562bd882d314f17d sio:SIO_000628 miriam-gene:1351, lld:C1282975;
    a sio:SIO_001121 .
}

dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_provenance {
  dgn-np:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_assertion dc:description
      "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. 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:9684781;
    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:NP372049.RABnW_Z9gzmb3oVsI0chfKqeD0ypwxWNUL7TwZPQVhdc0130_publicationInfo {
  this: dc:created "2014-10-02T12:35:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}