@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ> .
@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:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_head {
  this: np:hasAssertion dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion;
    np:hasProvenance dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance;
    np:hasPublicationInfo dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion a np:Assertion .
  
  dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance a np:Provenance .
  
  dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGN8d9810aa9a12f4f5ef5158630d423623 sio:SIO_000628 miriam-gene:1351, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_provenance {
  dgn-np:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_assertion dcterms:description
      "[Patients with CRF had a similar distribution to those with chronic liver diseases, whilst the greatest diversity of genotypes was seen in patients with haemophilia, which was expected since they were given factor VIII manufactured overseas.]. 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:9744672;
    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:NP849597.RAC4-fmdUt76OflM3w1NHG2PnkD44sDYZ2J6tCV0SNjXQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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" .
}