@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_head {
  this: np:hasAssertion dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_assertion;
    np:hasProvenance dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_provenance;
    np:hasPublicationInfo dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_assertion a np:Assertion .
  
  dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_provenance a np:Provenance .
  
  dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_assertion {
  miriam-gene:7035 a ncit:C16612 .
  
  lld:C0019069 a ncit:C7057 .
  
  dgn-gda:DGNd5d7e6df671e3e168418a2552bb5bf45 sio:SIO_000628 miriam-gene:7035, lld:C0019069;
    a sio:SIO_001121 .
}

dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_provenance {
  dgn-np:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_assertion dcterms:description
      "[Although it is difficult to speculate on the factors that might modify bleeding severity in patients with hemophilia, recent observations indicate that other coagulation proteins, such as tissue factor pathway inhibitor or polymorphisms in coagulation factor genes and genetic defects associated with hypercoagulability may account for the variability in clinical phenotype among patients with hemophilia.]. 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:23763284;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1085656.RAr407BJw0PNrtFul1Ciwh42qGY16NR5kRk7oolBVR0z0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:58+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}