@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI> .
@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:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_head {
  this: np:hasAssertion dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion;
    np:hasProvenance dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance;
    np:hasPublicationInfo dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion a np:Assertion .
  
  dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance a np:Provenance .
  
  dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion {
  miriam-gene:83886 a ncit:C16612 .
  
  lld:C0085669 a ncit:C7057 .
  
  dgn-gda:DGNe9b60752a519746fb6f687896eb6097a sio:SIO_000628 miriam-gene:83886, lld:C0085669;
    a sio:SIO_001121 .
}

dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_provenance {
  dgn-np:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_assertion dcterms:description
      "[Although previous candidate genetic studies have identified mutations in MPN patients who develop acute leukemia, the complement of genetic abnormalities in MPN patients who undergo LT is not known nor have specific molecular abnormalities been shown to have clinical relevance in this setting.]. 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:22431577;
    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:NP651314.RAuhiQ6nwcxTy8xcUhW8gtciNOOsH8R7TVn-uxw5TGQGI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:32+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" .
}