@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o> .
@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:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_head {
  this: np:hasAssertion dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_assertion;
    np:hasProvenance dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_provenance;
    np:hasPublicationInfo dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_assertion a np:Assertion .
  
  dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_provenance a np:Provenance .
  
  dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_assertion {
  miriam-gene:23564 a ncit:C16612 .
  
  lld:C1849472 a ncit:C7057 .
  
  dgn-gda:DGNbef5b406dd0211c785c08693a8530a7c sio:SIO_000628 miriam-gene:23564, lld:C1849472;
    a sio:SIO_001121 .
}

dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_provenance {
  dgn-np:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_assertion dcterms:description
      "[Based on the gene frequency of the 1529A mutation in the white population and on its relative abundance in patients with hemolytic anemia caused by PK deficiency, the prevalence of PK deficiency is estimated at 51 cases per million white population.]. 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:10828047;
    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:NP175837.RASN05s2evTOTF9hWfks9__wv0wFg8fY5dNNVvvnzJh9o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}