@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk> .
@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:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_head {
  this: np:hasAssertion dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_assertion;
    np:hasProvenance dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_provenance;
    np:hasPublicationInfo dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_assertion a np:Assertion .
  
  dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_provenance a np:Provenance .
  
  dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0042974 a ncit:C7057 .
  
  dgn-gda:DGN054693209a1aebc424f5fe93b55184e6 sio:SIO_000628 miriam-gene:7450, lld:C0042974;
    a sio:SIO_001121 .
}

dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_provenance {
  dgn-np:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_assertion dcterms:description
      "[Specific mutations within the von Willebrand factor gene have been identified in many of the qualitative variants of von Willebrand disease, providing important new insight into the structure and function of this central clotting protein.]. 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:23401896;
    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:NP168248.RAbzoNd_qLwLUaazkrWEhAPD98n6PJV_FCuCNLicWt9jk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}