@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70> .
@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:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_head {
  this: np:hasAssertion dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion;
    np:hasProvenance dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance;
    np:hasPublicationInfo dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion a np:Assertion .
  
  dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance a np:Provenance .
  
  dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  
  lld:C0005779 a ncit:C7057 .
  
  dgn-gda:DGNed1a611057d0b35244ab4cbb44205309 sio:SIO_000628 miriam-gene:1351, lld:C0005779;
    a sio:SIO_001121 .
}

dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_provenance {
  dgn-np:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_assertion dcterms:description
      "[Deficiencies of coagulation factors other than factor VIII and factor IX that cause bleeding disorders are inherited as autosomal recessive traits and are rare, with prevalences in the general population varying between 1 in 500 000 and 1 in 2 million for the homozygous forms.]. 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:15138162;
    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:NP443612.RAnjjW3pcqy_k82Xvd4QOi5WR-LrA7n8Y4vtnQFNlma70130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:06+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" .
}