@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI> .
@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:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_head {
  this: np:hasAssertion dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_assertion ;
    np:hasProvenance dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_provenance ;
    np:hasPublicationInfo dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_assertion a np:Assertion .
  dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_provenance a np:Provenance .
  dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_assertion {
  miriam-gene:3725 a ncit:C16612 .
  lld:C0002793 a ncit:C7057 .
  dgn-gda:DGN8c1853dd016b4ce4006f7ef928615cbc sio:SIO_000628 miriam-gene:3725 , lld:C0002793 ;
    a sio:SIO_001121 .
}
dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_provenance {
  dgn-np:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_assertion dcterms:description "[Of particular interest, amplicons containing genes involved in the c-jun NH2-terminal kinase/mitogen-activated protein kinase pathway, that is, JUN in 1p32 and MAP3K7IP2 (TAB2) in 6q24-25, were found to be independently amplified in eight of 11 cases with 12q amplification, providing strong support for the notion that aberrant expression of this pathway is an important step in the dedifferentiation of liposarcomas.]. 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:16732325 ;
    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:NP269964.RAeokq_9s_JaD9e-kiIn175psKnXqAJ03WQRr_E4YSZQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:30+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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}