@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U> .
@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:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_head {
  this: np:hasAssertion dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_assertion;
    np:hasProvenance dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_provenance;
    np:hasPublicationInfo dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_assertion a np:Assertion .
  
  dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_provenance a np:Provenance .
  
  dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_assertion {
  miriam-gene:171023 a ncit:C16612 .
  
  lld:C1292778 a ncit:C7057 .
  
  dgn-gda:DGNf1531670a81dcd518aadb1aee315901b sio:SIO_000628 miriam-gene:171023, lld:C1292778;
    a sio:SIO_001121 .
}

dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_provenance {
  dgn-np:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_assertion dcterms:description
      "[Our findings argue that the mutational order of events in MPN and sAML varies in different patients, and that TET2 and ASXL1 mutations have distinct roles in MPN pathogenesis and leukemic transformation.]. 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:20068184;
    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:NP763605.RAk0psxhNILI8BzTV246uKA_GX4clMc4-ed0_JicPT33U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+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" .
}