@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g> .
@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:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_head {
  this: np:hasAssertion dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion ;
    np:hasProvenance dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance ;
    np:hasPublicationInfo dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion a np:Assertion .
  dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance a np:Provenance .
  dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion {
  miriam-gene:3717 a ncit:C16612 .
  lld:C0398623 a ncit:C7057 .
  dgn-gda:DGN1a5888880bc50d7962ed7a9a21d11964 sio:SIO_000628 miriam-gene:3717 , lld:C0398623 ;
    a sio:SIO_001121 .
}
dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_provenance {
  dgn-np:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_assertion dcterms:description "[Accordingly, it seems that the investigation for the V617F mutation of the JAK2 gene is not mandatory in all Mexican mestizo patients with unexplained thrombophilia and that this genetic study should be reserved for special cases, such as patients with thrombosis in uncommon sites or patients with cell counts suggesting the presence of an underlying MPD.]. 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:18796251 ;
    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:NP553343.RA3ebTsvrkD3hYhnUW-LgeTnmgSkv-n-zMCLN8tRcnL8g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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: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" .
}