@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_head {
  this: np:hasAssertion dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_assertion;
    np:hasProvenance dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_provenance;
    np:hasPublicationInfo dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_assertion a np:Assertion .
  
  dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_provenance a np:Provenance .
  
  dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0280100 a ncit:C7057 .
  
  dgn-gda:DGN4a63accf4ced6d26c4910f7e3cea4503 sio:SIO_000628 miriam-gene:7157, lld:C0280100;
    a sio:SIO_001121 .
}

dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_provenance {
  dgn-np:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_assertion dcterms:description
      "[A single nucleotide polymorphism (SNP) at position 309 in the promoter region of MDM2 leading to increased expression of MDM2 and attenuated function of p53 has been negatively associated with onset and outcome of disease in solid tumors.]. 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:18467716;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP670088.RA41U9gDQsCYFUnkQcnRAlRQ2oMez9acaEPt1w1ZIutBI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:49+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}