@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ> .
@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:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_head {
  this: np:hasAssertion dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion;
    np:hasProvenance dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance;
    np:hasPublicationInfo dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion a np:Assertion .
  
  dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance a np:Provenance .
  
  dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion {
  miriam-gene:27115 a ncit:C16612 .
  
  lld:C0023434 a ncit:C7057 .
  
  dgn-gda:DGN09b85a9f9622601df7ae0661fcecf986 sio:SIO_000628 miriam-gene:27115, lld:C0023434;
    a sio:SIO_001121 .
}

dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance {
  dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion dcterms:description
      "[The low frequency of this 5' untranslated region variant indicates that it does not explain the higher PDE7B expression in patients with CLL but it has the potential to influence other settings that involve a role for PDE7B.]. 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:21796143;
    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:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:39+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: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" .
}