@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_head {
  this: np:hasAssertion dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_assertion;
    np:hasProvenance dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_provenance;
    np:hasPublicationInfo dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_assertion a np:Assertion .
  
  dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_provenance a np:Provenance .
  
  dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN172f7dd767bc4d7eaa127be2ac5333ad sio:SIO_000628 miriam-gene:2952, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_provenance {
  dgn-np:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_assertion dcterms:description
      "[The level of chromosome breaks (spontaneous and induced), the level of DNA damage (spontaneous and induced), DNA repair potential and the distribution of polymorphic variants of GSTT1 gene are not significantly different in YA and in OP, which suggests that these factors do not appear the causative factors for HNSCC in young age.]. 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:17653748;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP440966.RAIThsttrJj0azx7r27CgwpeGcuBT0nPpqM5VNQy6YrXU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:57+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}