@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo> .
@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:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_head {
  this: np:hasAssertion dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_assertion ;
    np:hasProvenance dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_provenance ;
    np:hasPublicationInfo dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_assertion a np:Assertion .
  dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_provenance a np:Provenance .
  dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGN87cba1cab5992209b72b1a6397639219 sio:SIO_000628 miriam-gene:1029 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_provenance {
  dgn-np:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_assertion dcterms:description "[Among the 3 cell cycle regulator proteins encoded at the 9p21 genetic locus, inactivation of p16 is the most frequent event in HCCs in which promoter hypermethylation and homozygous deletions are the common mechanisms.]. 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:10897001 ;
    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:NP289181.RAg-W8IIc5FKWXEc-cPpnmKf0CyjkXSCJ2kc8s1bJerQo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:56+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" .
}