@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4> .
@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:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_head {
  this: np:hasAssertion dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion;
    np:hasProvenance dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_provenance;
    np:hasPublicationInfo dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion a np:Assertion .
  
  dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_provenance a np:Provenance .
  
  dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN1cd225fa46aadb88567d71e9558f83e7 sio:SIO_000628 miriam-gene:3845, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_provenance {
  dgn-np:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_assertion dcterms:description
      "[Juvenile myelomonocytic leukemia (JMML) is an intractable pediatric leukemia with poor prognosis whose molecular pathogenesis is poorly understood, except for somatic or germline mutations of RAS pathway genes, including PTPN11, NF1, NRAS, KRAS and CBL, in the majority of cases.]. 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:23832011;
    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:NP430117.RADv_Ex5loz8ceGEizTnT9Al9rs3oxIsp6ddctQJupdX4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:15+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" .
}