@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs> .
@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:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_head {
  this: np:hasAssertion dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion;
    np:hasProvenance dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance;
    np:hasPublicationInfo dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion a np:Assertion .
  
  dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance a np:Provenance .
  
  dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion {
  miriam-gene:2130 a ncit:C16612 .
  
  lld:C0022665 a ncit:C7057 .
  
  dgn-gda:DGNc585be5d832d6bb7e666c0a0006d242f sio:SIO_000628 miriam-gene:2130, lld:C0022665;
    a sio:SIO_001121 .
}

dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_provenance {
  dgn-np:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_assertion dcterms:description
      "[As EWSR1 rearrangements are known to be a characteristic of Ewing tumors (ET), our findings illustrate the diagnostic problems regarding small cell kidney tumors and strongly argue for the need of adjuvant diagnostic techniques in this group of neoplasms.]. 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:18615675;
    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:NP550626.RAPjCEBXMWXUWv8d-13ncjYWcCmhnqddIO9L_AC_Xi8vs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}