@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_head {
  this: np:hasAssertion dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_assertion;
    np:hasProvenance dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_provenance;
    np:hasPublicationInfo dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_assertion a np:Assertion .
  
  dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_provenance a np:Provenance .
  
  dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_assertion {
  miriam-gene:79811 a ncit:C16612 .
  
  lld:C0026986 a ncit:C7057 .
  
  dgn-gda:DGNbb0509668e98eadf6581780de6f28190 sio:SIO_000628 miriam-gene:79811, lld:C0026986;
    a sio:SIO_001121 .
}

dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_provenance {
  dgn-np:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_assertion dcterms:description
      "[In addition to the detection of mutations known to be associated with MDS in NRAS, KRAS, MPL, NPM1, IDH1, PTPN11, APC and MET, single nucleotide variants so far unrelated to MDS in STK11 (n=1), KDR (n=3), ATM (n=1) and JAK3 (n=2) were identified.]. 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:24674452;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP945860.RAp9IdI8dP3SpqmEnIw9DNYK2wTQvr9u18XdkFlrfGxVc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:17+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}