@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs> .
@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:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_head {
  this: np:hasAssertion dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_assertion ;
    np:hasProvenance dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_provenance ;
    np:hasPublicationInfo dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_assertion a np:Assertion .
  dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_provenance a np:Provenance .
  dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_assertion {
  miriam-gene:728340 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGNff574d486bd5286c48b1b6969a3c093a sio:SIO_000628 miriam-gene:728340 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_provenance {
  dgn-np:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_assertion dcterms:description "[Together with the role of 19S subunits in transcriptional regulation, homology between S12 and eIF3 and TFIIH subunits, coelution with immunoproteasome subunits, and differential posttranslational modification and nuclear localization, these data suggest a differential nuclear function of modified and unmodified S12 in cancer.]. 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:15221960 ;
    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:NP878285.RAiT-RnZ3ZEux7axIB82ztvC5YSgSJ9b_S3OJ8h-DTzSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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: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" .
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}