@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw> .
@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:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_head {
  this: np:hasAssertion dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion;
    np:hasProvenance dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance;
    np:hasPublicationInfo dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion a np:Assertion .
  
  dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance a np:Provenance .
  
  dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion {
  miriam-gene:7450 a ncit:C16612 .
  
  lld:C0042974 a ncit:C7057 .
  
  dgn-gda:DGN87d9f84c60679ae80f62929647e4f0e5 sio:SIO_000628 miriam-gene:7450, lld:C0042974;
    a sio:SIO_001122 .
}

dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance {
  dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion dct:description
      "[In conclusion, the automated fluorescent capillary electrophoresis method presented here is an extremely rapid, simple and highly informative technique for association studies between VWD and the VWF gene in addition to genetic counseling and prenatal diagnosis by precise linkage analysis in VWD-affected families.]. 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:15886817;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}