@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA> .
@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:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_head {
  this: np:hasAssertion dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_assertion ;
    np:hasProvenance dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_provenance ;
    np:hasPublicationInfo dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_assertion a np:Assertion .
  dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_provenance a np:Provenance .
  dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_assertion {
  miriam-gene:3135 a ncit:C16612 .
  lld:C0279702 a ncit:C7057 .
  dgn-gda:DGN1b65dc50e1c3ff861608422fe447da5e sio:SIO_000628 miriam-gene:3135 , lld:C0279702 ;
    a sio:SIO_001121 .
}
dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_provenance {
  dgn-np:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_assertion dcterms:description "[These results provide evidence for the heterogeneity of major histocompatibility complex expression patterns in renal carcinoma and support the hypothesis that specific mechanisms underlying the malignant transformation into clear cell renal carcinoma up-regulate expression of HLA-G and to a lesser extent HLA class II molecule expression.]. 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:12547708 ;
    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:NP891778.RA51mVE7jinHq_P-DBhCcyyyBkmELRfGbuNxLUZ1A_ajA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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 ;
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    pav:version "v2.1.0.0" .
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}