@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY> .
@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:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_head {
  this: np:hasAssertion dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_assertion;
    np:hasProvenance dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_provenance;
    np:hasPublicationInfo dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_assertion a np:Assertion .
  
  dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_provenance a np:Provenance .
  
  dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_assertion {
  miriam-gene:613 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGN3f76fda19e4fe96009a455001b9d11ec sio:SIO_000628 miriam-gene:613, lld:C0001815;
    a sio:SIO_001121 .
}

dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_provenance {
  dgn-np:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_assertion dcterms:description
      "[We report an elderly patient who presented with primary myelofibrosis (MF) with myeloid metaplasia (MMM), associated with idic(17)(p11.2) as the sole chromosomal abnormality, making this the first idic(17)(p11.2) myeloproliferative case reported in which the breakpoints are mapped to the breakpoint cluster region in proximal 17p.]. 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:16044457;
    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:NP871893.RAWDH5UJUQTraSihZ5DZNTdRmXKLypVU6Gip6ft5KfxVY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:53+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" .
}