@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes> .
@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:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_head {
  this: np:hasAssertion dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion;
    np:hasProvenance dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance;
    np:hasPublicationInfo dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion a np:Assertion .
  
  dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance a np:Provenance .
  
  dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN633ab2a592d02e3c647c516c600c1a54 sio:SIO_000628 miriam-gene:5925, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance {
  dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion dcterms:description
      "[Thus, it seems that the putative TSGs located in the BRCAX and 13q31.1 regions as well as the BRCA2 and RB1 genes may have some cumulative effect in progression and poor prognosis of HNSCC.]. 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:16623759;
    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:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:55+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" .
}