@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ> .
@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:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_head {
  this: np:hasAssertion dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion ;
    np:hasProvenance dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion a np:Assertion .
  dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance a np:Provenance .
  dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion {
  miriam-gene:2056 a ncit:C16612 .
  lld:C1318533 a ncit:C7057 .
  dgn-gda:DGNa53b40408653cd4aef6d9014df797aa9 sio:SIO_000628 miriam-gene:2056 , lld:C1318533 ;
    a sio:SIO_001121 .
}
dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_provenance {
  dgn-np:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_assertion dcterms:description "[Absolute erythrocytoses are divided into primary, where the erythropoietic compartment is intrinsically abnormal, secondary, where the erythropoietic compartment is normal but is responding to external pathological events leading to an increased erythropoietin drive, and idiopathic, where neither a primary nor a secondary erythrocytosis can be established.]. 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:10640213 ;
    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:NP889999.RAhn1NKivFSuOEdRiI1dnA5Lj-WQsVh-0IhM_7p_n2rNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}