@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk> .
@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:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_head {
  this: np:hasAssertion dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion;
    np:hasProvenance dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance;
    np:hasPublicationInfo dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion a np:Assertion .
  
  dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance a np:Provenance .
  
  dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN107f5bb494b4daa6366b3b84f9c09501 sio:SIO_000628 miriam-gene:3717, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance {
  dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion dcterms:description
      "[A point mutation in the Janus tyrosine kinase 2 (JAK2) gene has been described in patients with chronic myeloproliferative disorders (MPD), but the clinical significance of JAK2(V617F), which may be harbored in either the heterozygote or homozyote status, is still largely undefined.]. 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:16572198;
    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:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}