@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE> .
@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:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_head {
  this: np:hasAssertion dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion ;
    np:hasProvenance dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance ;
    np:hasPublicationInfo dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion a np:Assertion .
  dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance a np:Provenance .
  dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion {
  miriam-gene:8731 a ncit:C16612 .
  lld:C1457883 a ncit:C7057 .
  dgn-gda:DGN60d2008e909d9daa01149ecd52e5d396 sio:SIO_000628 miriam-gene:8731 , lld:C1457883 ;
    a sio:SIO_001121 .
}
dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_provenance {
  dgn-np:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_assertion dcterms:description "[In primary myxofibrosarcomas, MET overexpression, as a frequent event, is likely driven by 7q gains with mRNA upregulation, associated with important prognosticators, and independently predictive of worse outcomes, highlighting its possible causative function in tumor aggressiveness and potentiality as a therapeutic target.]. 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:20639860 ;
    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:NP893111.RAJT5661ID2R0BpqXeBAa5BZLSY_V6x04k_OIsD0xcHLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+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" .
}