@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k> .
@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:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_head {
  this: np:hasAssertion dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion;
    np:hasProvenance dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance;
    np:hasPublicationInfo dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion a np:Assertion .
  
  dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance a np:Provenance .
  
  dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C0027022 a ncit:C7057 .
  
  dgn-gda:DGN8d2c73920d6230d90c8e95eb274b1cf2 sio:SIO_000628 miriam-gene:3717, lld:C0027022;
    a sio:SIO_001122 .
}

dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance {
  dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion dcterms:description
      "[ARMS-PCR technique can be used to detect the frequency and mutational status of JAK2V617F mutation owing to its sensitivity and along with capillary electrophoresis, quantitative assay for mutated JAK2 mRNA, diagnosis of CMPD and judgement of prognosis become possible.]. 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:19549471;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:34+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" .
}