@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q> .
@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:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_head {
  this: np:hasAssertion dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion ;
    np:hasProvenance dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion a np:Assertion .
  dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance a np:Provenance .
  dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  lld:C0040038 a ncit:C7057 .
  dgn-gda:DGNc9c20228f6c3b3d4f41c95a1c71d6997 sio:SIO_000628 miriam-gene:3717 , lld:C0040038 ;
    a sio:SIO_001121 .
}
dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_provenance {
  dgn-np:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_assertion dcterms:description "[Furthermore, patients affected by essential thrombocythemia who are carriers of the Janus kinase 2 Val617Phe mutation show a higher incidence of venous thromboembolism both before, and at the time of diagnosis, compared with noncarriers, and recent evidence of splanchnic and cerebral vein thrombosis in carriers of the Janus kinase 2 Val617Phe mutation has been reported.]. 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:18600099 ;
    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:NP491706.RAMtMxyFviPI4LB70tA_mT6EG98YnDz3jE7mkpGNieh9Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:53+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" .
}