@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA> .
@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:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_head {
  this: np:hasAssertion dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_assertion;
    np:hasProvenance dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_provenance;
    np:hasPublicationInfo dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_assertion a np:Assertion .
  
  dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_provenance a np:Provenance .
  
  dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_assertion {
  miriam-gene:3815 a ncit:C16612 .
  
  lld:C0079772 a ncit:C7057 .
  
  dgn-gda:DGN91d0940dc0ec04d0dfa4db24f0b18afc sio:SIO_000628 miriam-gene:3815, lld:C0079772;
    a sio:SIO_001121 .
}

dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_provenance {
  dgn-np:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_assertion dcterms:description
      "[Gain-of-function KIT mutations are usually acquired and have been associated with myeloid malignancies including core binding factor acute myeloid leukemia and systemic mastocytosis (SM), germ cell tumors, gastrointestinal stromal tumors and sinonasal T cell lymphomas.]. 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:18566536;
    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:NP240560.RAZTmUuZy0JHlpoRgOnKkG0xCrMF2LWYx6GwsOSlS76yA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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" .
}