@prefix semsc: <http://semanticscience.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@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 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:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_head {
  this: np:hasAssertion dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion;
    np:hasProvenance dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance;
    np:hasPublicationInfo dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion a np:Assertion .
  
  dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance a np:Provenance .
  
  dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion {
  miriam-gene:23417 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN2f7f8ddde37e25f2d81445389d2eb839 semsc:SIO_000628 miriam-gene:23417, lld:C0006826;
    a semsc:SIO_001121 .
}

dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance {
  dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion dct:description
      "[Since not all gene expression changes observed in a tumor are causal to cancer development, we demonstrate an approach based on multiple concerted disruption (MCD) analysis of genes that facilitates the rational deduction of aberrant genes and pathways, which otherwise would be overlooked in single genomic dimension investigations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    semsc:SIO_000772 miriam-pubmed:20478067;
    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:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo {
  this: dct:created "2014-10-02T12:33:53+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject semsc:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}