@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s> .
@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:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_head {
  this: np:hasAssertion dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_assertion;
    np:hasProvenance dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_provenance;
    np:hasPublicationInfo dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_assertion a np:Assertion .
  
  dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_provenance a np:Provenance .
  
  dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_assertion {
  miriam-gene:1869 a ncit:C16612 .
  
  lld:C0007121 a ncit:C7057 .
  
  dgn-gda:DGNd2c307890a53299fe1aefd7b7303db33 sio:SIO_000628 miriam-gene:1869, lld:C0007121;
    a sio:SIO_001121 .
}

dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_provenance {
  dgn-np:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_assertion dcterms:description
      "[p21 TA levels vary considerably among BC patients which may be attributable to 1) genetic alterations in Rb and p53 and 2) variation in TA levels of upstream transcription factors E2F1 and p73.]. 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:16014176;
    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:NP825632.RAM8Yc6FR-wkVODvx5Bnc0Y-vuVJkqRQssfHmDr7UCr9s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:25+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" .
}