@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4> .
@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:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_head {
  this: np:hasAssertion dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion;
    np:hasProvenance dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance;
    np:hasPublicationInfo dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion a np:Assertion .
  
  dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance a np:Provenance .
  
  dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion {
  miriam-gene:1719 a ncit:C16612 .
  
  lld:C0029463 a ncit:C7057 .
  
  dgn-gda:DGN5336da1f420845c99e8d6e02b1575911 sio:SIO_000628 miriam-gene:1719, lld:C0029463;
    a sio:SIO_001121 .
}

dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_provenance {
  dgn-np:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_assertion dcterms:description
      "[The assessment of C-MYC and DHFR at diagnosis, together with that of other known prognostic markers, can be considered for an early identification of subgroups of OS patients with higher risk of adverse outcome.]. 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:18385200;
    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:NP889618.RAlNCUiPIif3fE5537U0YCziLF2xWrCm29DaUnyYcYmd4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:07+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" .
}