@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8> .
@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:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_head {
  this: np:hasAssertion dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_assertion;
    np:hasProvenance dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_provenance;
    np:hasPublicationInfo dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_assertion a np:Assertion .
  
  dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_provenance a np:Provenance .
  
  dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_assertion {
  miriam-gene:5524 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN826f79164c32bf7151bdc8a5685ed949 sio:SIO_000628 miriam-gene:5524, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_provenance {
  dgn-np:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_assertion dcterms:description
      "[Although the frequency of alterations is low, the inclusion of both isoforms of subunit A in the genes mutated in human cancer and the addition of breast cancer to the list of neoplasms in which PPP2R1B is altered, strengthen the potential role of PP2A in human tumorogenesis.]. 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:10713707;
    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:NP230138.RA72LDAYLBIJ4-wrafFbSNgRMY6MiC3_7ubhUx5Y3cJV8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:09+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" .
}