@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI> .
@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:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_head {
  this: np:hasAssertion dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_assertion;
    np:hasProvenance dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_provenance;
    np:hasPublicationInfo dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_assertion a np:Assertion .
  
  dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_provenance a np:Provenance .
  
  dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_assertion {
  miriam-gene:10278 a ncit:C16612 .
  
  lld:C0700095 a ncit:C7057 .
  
  dgn-gda:DGN5964f8df1ca94148f2c04ce1910c7c88 sio:SIO_000628 miriam-gene:10278, lld:C0700095;
    a sio:SIO_001121 .
}

dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_provenance {
  dgn-np:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_assertion dcterms:description
      "[Furthermore, our analysis showed that high WEE1 levels are significantly associated with poor EFS and OS in neuroblastoma and that siRNA knockdown of WEE1 in MNA cell lines results in significant levels of apoptosis, supporting an oncogenic role of WEE1 in neuroblastoma.]. 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:23531080;
    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:NP896343.RA1ZLqi5INoONLxqjGTtuVJ4270mYq6Y-ktoO5sn_oYyI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:11+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" .
}