@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE> .
@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:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_head {
  this: np:hasAssertion dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_assertion;
    np:hasProvenance dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_provenance;
    np:hasPublicationInfo dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_assertion a np:Assertion .
  
  dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_provenance a np:Provenance .
  
  dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0272355 a ncit:C7057 .
  
  dgn-gda:DGN9ac26a1f4e0b806c20a8085fc08e46a5 sio:SIO_000628 miriam-gene:7450, lld:C0272355;
    a sio:SIO_001121 .
}

dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_provenance {
  dgn-np:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_assertion dcterms:description
      "[A screening project to identify candidate molecular defects causing von Willebrand disease type IIC (VWD IIC) in a German family was carried out using polymerase chain reaction (PCR) amplification of all 52 exons of the von Willebrand factor (VWF) gene, subsequent electrophoresis of single and double stranded DNA and direct sequencing of PCR products with aberrant electrophoretic patterns.]. 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:7789955;
    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:NP196198.RAj3miseacW2FunrJjjAtBK-dzzlZLF7xOlTdZdj4UxmE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:48+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" .
}