@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA> .
@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:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_head {
  this: np:hasAssertion dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_assertion;
    np:hasProvenance dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_provenance;
    np:hasPublicationInfo dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_assertion a np:Assertion .
  
  dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_provenance a np:Provenance .
  
  dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_assertion {
  miriam-gene:1493 a ncit:C16612 .
  
  lld:C0278996 a ncit:C7057 .
  
  dgn-gda:DGN020f7f2cd717d537af3cb77ae154a00c sio:SIO_000628 miriam-gene:1493, lld:C0278996;
    a sio:SIO_001121 .
}

dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_provenance {
  dgn-np:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_assertion dcterms:description
      "[From the published literature, we identified 23 germ line sequence variants in 17 genes from hypothesis-generating studies that were associated with prognosis of head and neck cancer, including sequence variants of DNA repair (ERCC1, ERCC4, ERCC5, MSH2, XPA, ERCC2, XRCC1, XRCC3), DNA methylation (DNMT3B), cell cycle and proliferation (CCND1, TP53), xenobiotic metabolism (GSTM1, GSTT1, CYP2D6), metastatic -potential (MMP3), immunologic (CTLA4), and growth factor pathways (FGFR4).]. 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:22076708;
    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:NP723044.RAF3hTyNeDMXUucXpcolTh_Uk4b4gNFKaw9LQkEfa6jcA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}