@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY> .
@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:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_head {
  this: np:hasAssertion dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_assertion ;
    np:hasProvenance dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_provenance ;
    np:hasPublicationInfo dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_assertion a np:Assertion .
  dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_provenance a np:Provenance .
  dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_assertion {
  miriam-gene:6790 a ncit:C16612 .
  lld:C0027627 a ncit:C7057 .
  dgn-gda:DGN532e47add856ad82ab053828b3647b2d sio:SIO_000628 miriam-gene:6790 , lld:C0027627 ;
    a sio:SIO_001121 .
}
dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_provenance {
  dgn-np:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_assertion dcterms:description "[CNA in the primary sites was more extensive in the GISTs with recurrence and metastasis than in those without, especially as to the loss of chromosome 20 and genomic imbalance of AURKA-containing BAC probe on 20q in the cases with metastasis.]. 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:16452129 ;
    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:NP165338.RAI4u4YzqywOs2MR1YeTNjTSnYQ6xHw5uJT_duaJGxfMY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}