@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM> .
@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:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_head {
  this: np:hasAssertion dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion;
    np:hasProvenance dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance;
    np:hasPublicationInfo dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion a np:Assertion .
  
  dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance a np:Provenance .
  
  dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion {
  miriam-gene:4005 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN46709e1910365b8b121f880908d423cb sio:SIO_000628 miriam-gene:4005, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance {
  dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion dcterms:description
      "[The highly concordant nature of the genetic events giving rise to mouse and human leukemias with mutations at Lmo2 are an encouraging sign to those wanting to use mice to model human cancer and may help in designing safer methods for retroviral gene therapy.]. 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:19461887;
    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:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:46+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" .
}