@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU> .
@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:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_head {
  this: np:hasAssertion dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_assertion;
    np:hasProvenance dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_provenance;
    np:hasPublicationInfo dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_assertion a np:Assertion .
  
  dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_provenance a np:Provenance .
  
  dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0278996 a ncit:C7057 .
  
  dgn-gda:DGN2fa66a36ccc7ba92e481d22205e81c07 sio:SIO_000628 miriam-gene:595, lld:C0278996;
    a sio:SIO_001121 .
}

dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_provenance {
  dgn-np:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_assertion dcterms:description
      "[Polymorphisms of XRCC1, FGFR, and CCND1 have been consistently associated with HNC survival in at least two studies, whereas most of the other polymorphisms have either conflicting data or were from single studies.]. 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:18349267;
    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:NP497423.RABXntz6blq4v1YsPPftgnx0HfShbTsDAlQi8HrUn-KlU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:56+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" .
}