@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I> .
@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:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_head {
   this: np:hasAssertion dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_assertion ;
    np:hasProvenance dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_provenance ;
    np:hasPublicationInfo dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_assertion a np:Assertion .
  dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_provenance a np:Provenance .
  dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_assertion {
   miriam-gene:4609 a ncit:C16612 .
  lld:C1458156 a ncit:C7057 .
  dgn-gda:DGNe7454e5da80285d0551f5a17f38a600d sio:SIO_000628 miriam-gene:4609 , lld:C1458156 ;
    a sio:SIO_001121 .
}
dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_provenance {
   dgn-np:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_assertion dcterms:description "[To identify genetic alterations associated with local recurrence risk in breast carcinoma, we analyzed 28 local recurrences and 173 primary breast tumors for the ten most frequently altered genetic regions in breast carcinomas, i.e., loss of heterozygosity on chromosomal arms 1p, 3p, 7q, 11p, 17p, 17q, and 18q, and amplification of the MYC and ERBB2 protooncogenes and of genes in 11q13.]. 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:7535085 ;
    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:NP811458.RAHVOtp9JJKXLiteRdx-hTDWKJH6bGACVebO3Po-NzF3I130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:17+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> ;
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}