@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo> .
@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:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_head {
  this: np:hasAssertion dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion;
    np:hasProvenance dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance;
    np:hasPublicationInfo dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion a np:Assertion .
  
  dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance a np:Provenance .
  
  dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGN190f2a12e1bd5161e6ffae1d837e2c47 sio:SIO_000628 miriam-gene:595, lld:C0007137;
    a sio:SIO_001122 .
}

dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance {
  dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion dcterms:description
      "[Because CCND1 plays a critical role in cell cycle control and reduced DNA repair capacity is associated with an increased risk for squamous cell carcinoma of the head and neck (SCCHN), we hypothesize that this CCND1 polymorphism modulates individual susceptibility to SCCHN.]. 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:11470749;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}