@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY> .
@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:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_head {
  this: np:hasAssertion dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_assertion ;
    np:hasProvenance dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_provenance ;
    np:hasPublicationInfo dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_assertion a np:Assertion .
  dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_provenance a np:Provenance .
  dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_assertion {
  miriam-gene:1520 a ncit:C16612 .
  lld:C0026769 a ncit:C7057 .
  dgn-gda:DGN265d10016ab435ddc453be0e7b66efd4 sio:SIO_000628 miriam-gene:1520 , lld:C0026769 ;
    a sio:SIO_001122 .
}
dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_provenance {
  dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_assertion dcterms:description "[Our work confirms and extends previous indications for a polygenic mechanism involved in bringing about responsiveness to recombinant IFN-beta. The identification of 2 genes active in the antigen processing and presentation cascade; that is, LMP7, coding for the proteasome subunit beta, and CTSS, coding for cathepsin S; as potential response modifiers may identify this pathway as being of particular relevance to phenotypic expression of response heterogeneity.]. 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:16338279 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP64148.RA8Ttp8KnOuAa22wdq-DptRTaGF92p3kctHw9saZY9UsY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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