@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw> .
@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:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_head {
  this: np:hasAssertion dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_assertion;
    np:hasProvenance dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_provenance;
    np:hasPublicationInfo dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_assertion a np:Assertion .
  
  dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_provenance a np:Provenance .
  
  dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_assertion {
  miriam-gene:3251 a ncit:C16612 .
  
  lld:C1527405 a ncit:C7057 .
  
  dgn-gda:DGNb9860406efde83dd5d6f2a54f06bb10e sio:SIO_000628 miriam-gene:3251, lld:C1527405;
    a sio:SIO_001121 .
}

dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_provenance {
  dgn-np:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_assertion dcterms:description
      "[X-chromosome DNA probes for the phosphoglycerate kinase (PGK) and hypoxanthine phosphoribosyl transferase (HPRT) genes were used to study clonality in haemopoietic cells from 63 women with myeloproliferative disease, idiopathic erythrocytosis, secondary erythrocytosis or normal red cell volumes.]. 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:2775657;
    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:NP1296708.RA3NQOKLrGs79fOaYe5NHvG9DdIeHkW4Ou0SH9OiNrVCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:33+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" .
}