@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs> .
@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:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_head {
  this: np:hasAssertion dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_assertion ;
    np:hasProvenance dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_provenance ;
    np:hasPublicationInfo dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_assertion a np:Assertion .
  dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_provenance a np:Provenance .
  dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  lld:C0023473 a ncit:C7057 .
  dgn-gda:DGN357fc0e5db347048abb5e5f17ab94905 sio:SIO_000628 miriam-gene:3133 , lld:C0023473 ;
    a sio:SIO_001121 .
}
dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_provenance {
  dgn-np:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_assertion dcterms:description "[We hypothesized that if antigen processing of the P210 fusion protein leads to presentation of peptides from the fusion region by major histocompatibility complex (MHC) molecules in vivo, this may be reflected in a diminished incidence of CML in individuals expressing HLA-A3, -A11, or -B8.]. 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:10339494 ;
    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:NP883160.RA0x2NJR1f_3HIvBexXqyr6zaKRkm6wnTrXfxPqmM82Rs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}