@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g> .
@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:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_head {
  this: np:hasAssertion dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion;
    np:hasProvenance dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance;
    np:hasPublicationInfo dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion a np:Assertion .
  
  dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance a np:Provenance .
  
  dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNf20154350315b06e3acff54220b27ff0 sio:SIO_000628 miriam-gene:1029, lld:C1956346;
    a sio:SIO_001121 .
}

dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_provenance {
  dgn-np:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_assertion dcterms:description
      "[The results of this study indicate that the 9p21 variation has an impact on CDKN2A and CDKN2B expression in VSMCs and influences VMSC proliferation, which likely represents an important mechanism for the association between this genetic locus and susceptibility to CAD.]. 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:22706276;
    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:NP990809.RAmO_hUvnqNG37IYoyCCAnuOOpCasUAUtJYTCkbj_KD6g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:14+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}