@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg> .
@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:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_head {
  this: np:hasAssertion dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion;
    np:hasProvenance dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance;
    np:hasPublicationInfo dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion a np:Assertion .
  
  dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance a np:Provenance .
  
  dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion {
  miriam-gene:54790 a ncit:C16612 .
  
  lld:C0026985 a ncit:C7057 .
  
  dgn-gda:DGN3dc9ab9b740651ac78b51c7f40cc79e6 sio:SIO_000628 miriam-gene:54790, lld:C0026985;
    a sio:SIO_001121 .
}

dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_provenance {
  dgn-np:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_assertion dcterms:description
      "[A new study reports common mutations in the TET2 gene in myelodysplasia and related myeloid malignancies, suggesting that TET2 has an important role in hematopoiesis and in the pathogenesis of this disease.]. 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:19557078;
    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:NP741061.RA10WEsObDH93MzlIkCEP-rnksXpPYgXfkAHNoMQPwHrg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:29+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" .
}