@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k> .
@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:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_head {
  this: np:hasAssertion dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_assertion;
    np:hasProvenance dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_provenance;
    np:hasPublicationInfo dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_assertion a np:Assertion .
  
  dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_provenance a np:Provenance .
  
  dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_assertion {
  miriam-gene:7764 a ncit:C16612 .
  
  lld:C1335475 a ncit:C7057 .
  
  dgn-gda:DGN55772bda218ce95f0f79c2dfcc1d74cc sio:SIO_000628 miriam-gene:7764, lld:C1335475;
    a sio:SIO_001121 .
}

dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_provenance {
  dgn-np:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_assertion dcterms:description
      "[To establish the frequency of 20q13 amplification and select the amplified cases to be studied, we used fluorescence in situ hybridization of bacterial artificial chromosome probes for three 20q13 loci (MYBL2, STK6, ZNF217) on sections of tissue microarrays containing 466 primary carcinoma samples.]. 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:16899599;
    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:NP857535.RAR_ejHJ06T7XxOifn4x_yllvIosvBdNp8IllbwDhxh1k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}