@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY> .
@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:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_head {
  this: np:hasAssertion dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_assertion;
    np:hasProvenance dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_provenance;
    np:hasPublicationInfo dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_assertion a np:Assertion .
  
  dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_provenance a np:Provenance .
  
  dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_assertion {
  miriam-gene:2160 a ncit:C16612 .
  
  lld:C0005779 a ncit:C7057 .
  
  dgn-gda:DGN4eb31a6e4ae39cb6af7c79c8902abaf7 sio:SIO_000628 miriam-gene:2160, lld:C0005779;
    a sio:SIO_001121 .
}

dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_provenance {
  dgn-np:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_assertion dcterms:description
      "[Defects in platelets as well as inherited deficiencies of coagulation factors including fibrinogen, FII, FV, FV + FVIII, FVII, FX, FXI and FXIII deficiencies, generally lead to lifelong bleeding disorders, whose severity of bleeding symptoms is heterogeneous in platelets abnormalities but generally inversely proportional to the degree of the factor deficiency in rare bleeding disorders (RBDs).]. 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:18510543;
    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:NP673869.RApegsnTpHR7JVGpDfoD3nnjdivTY3huG15GreRvUXtcY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:50+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" .
}