@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28> .
@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:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_head {
  this: np:hasAssertion dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_assertion;
    np:hasProvenance dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_provenance;
    np:hasPublicationInfo dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_assertion a np:Assertion .
  
  dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_provenance a np:Provenance .
  
  dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_assertion {
  miriam-gene:2056 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGN8448404eaaa3dd2a4af199ffb4eb005b sio:SIO_000628 miriam-gene:2056, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_provenance {
  dgn-np:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_assertion dcterms:description
      "[Although none of these 10 cases have developed overt clinical and laboratory features of such a myeloproliferative disorder after a median observation period of two years, the presence of clonal karyotypic abnormalities in three cases, increased megakaryocyte colony growth in three cases and endogenous erythropoietin independent colony growth of the marrow erythroid progenitors in seven cases, argues strongly in favour of a primary haematological disorder.]. 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:2236481;
    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:NP577683.RAV8wt9FOYiHr8bFDW7kbOhKd5FG90rMjsMGt_aPNol28130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:48+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" .
}