@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA> .
@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:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_head {
  this: np:hasAssertion dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion;
    np:hasProvenance dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance;
    np:hasPublicationInfo dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion a np:Assertion .
  
  dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance a np:Provenance .
  
  dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C1282975 a ncit:C7057 .
  
  dgn-gda:DGN98cd2ba1028a46993bde6efe33ca41f5 sio:SIO_000628 miriam-gene:7450, lld:C1282975;
    a sio:SIO_001121 .
}

dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_provenance {
  dgn-np:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_assertion dcterms: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:NP620726.RAmcK4vpgZSC-TdzWcJxlsUH6ceBlCUYQZHKC8awaj9LA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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" .
}