@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE> .
@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:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_head {
  this: np:hasAssertion dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_assertion ;
    np:hasProvenance dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_provenance ;
    np:hasPublicationInfo dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_assertion a np:Assertion .
  dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_provenance a np:Provenance .
  dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_assertion {
  miriam-gene:23600 a ncit:C16612 .
  lld:C1333064 a ncit:C7057 .
  dgn-gda:DGN12ff403144103cd13a023b80b33a2416 sio:SIO_000628 miriam-gene:23600 , lld:C1333064 ;
    a sio:SIO_001121 .
}
dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_provenance {
  dgn-np:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_assertion dcterms:description "[In comparison to the germinal center profiles, the most frequent imbalances in HL were losses in 5p13 (AMACR, GDNF, and SKP2), and gains in 7q36 (SHH, sonic hedgehog homolog) and 9q34 (ABL1, CDK9, LCN2, and PTGES).]. 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:21385932 ;
    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:NP469660.RAGedKllyA_tH5L_8jXgLbWsfY88CSp9nhjCnlWkL3McE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:41+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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}