@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM> .
@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:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_head {
  this: np:hasAssertion dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion ;
    np:hasProvenance dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance ;
    np:hasPublicationInfo dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion a np:Assertion .
  dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance a np:Provenance .
  dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion {
  miriam-gene:7301 a ncit:C16612 .
  lld:C0006142 a ncit:C7057 .
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}
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance {
  dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion dcterms:description "[To characterize the genomic instability observed in these tumors, to establish a comparative map of chromosomal imbalances and to contribute to the validation of this mouse model of breast cancer, we have characterized chromosomal imbalances and aberrations using comparative genomic hybridization (CGH), and spectral karyotyping (SKY).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}