@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI> .
@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/v3.0.0/void/> .

dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_head {
  this: np:hasAssertion dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion;
    np:hasProvenance dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance;
    np:hasPublicationInfo dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion a np:Assertion .
  
  dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance a np:Provenance .
  
  dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion {
  miriam-gene:3704 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGNe714ef25d73bf57e1792880b022e8eee sio:SIO_000628 miriam-gene:3704, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_provenance {
  dgn-np:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_assertion dcterms:description
      "[We hypothesize that patients (63%) being homozygous for both major alleles, leading to normal ITPase activity, may benefit more from the addition of ribavirin to present and future treatment regimens for HCV in spite of concomitant increased risk of anemia.]. 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:24519039;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP518635.RAjqpgCQf8Mp0mcSH-na5Twhbf632sowwGLVOPvDhf7UI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:46+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}