@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50> .
@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:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_head {
  this: np:hasAssertion dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_assertion;
    np:hasProvenance dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_provenance;
    np:hasPublicationInfo dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_assertion a np:Assertion .
  
  dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_provenance a np:Provenance .
  
  dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_assertion {
  miriam-gene:867 a ncit:C16612 .
  
  lld:C0280449 a ncit:C7057 .
  
  dgn-gda:DGN3221e7e099e840e282236503859464d1 sio:SIO_000628 miriam-gene:867, lld:C0280449;
    a sio:SIO_001122 .
}

dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_provenance {
  dgn-np:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_assertion dcterms:description
      "[In particular the detection and quantification of a copy-neutral loss of heterozygosity region located in chromosome 11q guided the search for point mutations in the CBL gene, thus allowing the escription of the novel missense mutation K382E and the demonstration of its selection during progression to secondary AML.]. 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:20674974;
    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:NP286394.RAlIyMpwBAHgWOMzj3PqP-vNx6hR1O3xvCCu-Llfcqg50130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:23+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" .
}