@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k> .
@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:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_head {
  this: np:hasAssertion dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion;
    np:hasProvenance dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance;
    np:hasPublicationInfo dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion a np:Assertion .
  
  dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance a np:Provenance .
  
  dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion {
  miriam-gene:4830 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN34221427b0dda58a59fdd68b604ae421 sio:SIO_000628 miriam-gene:4830, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_provenance {
  dgn-np:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_assertion dcterms:description
      "[To study genetic alterations related to the development and/or progression of breast carcinoma, we examined amplification of the ERBB2, INT2, and MYC genes, as well as loss of heterozygosity (LOH) at loci on 11p, 16q, 17p (D17S5 and TP53), 17q (D17S74 and NME1), and 18q by restriction fragment length polymorphism analysis.]. 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:7903963;
    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:NP928201.RAkU27DwYoDTdw2zRCM7NO6a5V3tifNyOL40wG4PfIr_k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:29+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" .
}