@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44> .
@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:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_head {
  this: np:hasAssertion dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_assertion;
    np:hasProvenance dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_provenance;
    np:hasPublicationInfo dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_assertion a np:Assertion .
  
  dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_provenance a np:Provenance .
  
  dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_assertion {
  miriam-gene:8289 a ncit:C16612 .
  
  lld:C0853879 a ncit:C7057 .
  
  dgn-gda:DGNd1e3d0f4f537be2e40486d816d16f725 sio:SIO_000628 miriam-gene:8289, lld:C0853879;
    a sio:SIO_001121 .
}

dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_provenance {
  dgn-np:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_assertion dcterms:description
      "[The influence of mutation and copy number variation on the expression were statistically insignificant at mRNA level, and were, therefore, not considered the main causes for ARID1A mRNA low expression in invasive breast cancer.]. 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:23349767;
    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:NP850138.RAiRSxmWiLh2qV7RXRZDM_htk6Mevu8W13gTlQbBncl44130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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" .
}