@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY> .
@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:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_head {
  this: np:hasAssertion dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion;
    np:hasProvenance dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance;
    np:hasPublicationInfo dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion a np:Assertion .
  
  dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance a np:Provenance .
  
  dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion {
  miriam-gene:83886 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGNa0d1debd7410298409a6c2bbe2cdca98 sio:SIO_000628 miriam-gene:83886, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_provenance {
  dgn-np:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_assertion dcterms:description
      "[Mutations in the Cbl family RING finger domain or linker sequence constitute important pathogenic lesions associated with not only preleukemic CMML, JMML, and other MPN, but also progression to AML, suggesting that impairment of degradation of activated tyrosine kinases constitutes an important cancer mechanism.]. 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:19901108;
    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:NP552694.RAJTNdehWNgR1XaQhGQiGlo18JOmcAAqOtZTY_V9-cqdY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:33+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" .
}