@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA> .
@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/v3.0.0/void/> .
dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_head {
   this: np:hasAssertion dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_assertion ;
    np:hasProvenance dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_provenance ;
    np:hasPublicationInfo dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_assertion a np:Assertion .
  dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_provenance a np:Provenance .
  dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_assertion {
   miriam-gene:153090 a ncit:C16612 .
  lld:C0003486 a ncit:C7057 .
  dgn-gda:DGNb9dd9da0dd0073e239dbb90c8eacbff3 sio:SIO_000628 miriam-gene:153090 , lld:C0003486 ;
    a sio:SIO_001121 .
}
dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_provenance {
   dgn-np:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_assertion dcterms:description "[The two genes with the strongest supporting evidence of contribution to the genetic risk for AAA are the CDKN2BAS gene, also known as ANRIL, which encodes an antisense ribonucleic acid that regulates expression of the cyclin-dependent kinase inhibitors CDKN2A and CDKN2B, and DAB2IP, which encodes an inhibitor of cell growth and survival.]. 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:21146954 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP976398.RAW4R9dw8TGUXk9Jq1AbwwCxLDxqrVE1hlTQl8uLEcSrA130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:36+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}