@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs> .
@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:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_head {
  this: np:hasAssertion dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_assertion;
    np:hasProvenance dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_provenance;
    np:hasPublicationInfo dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_assertion a np:Assertion .
  
  dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_provenance a np:Provenance .
  
  dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_assertion {
  miriam-gene:63036 a ncit:C16612 .
  
  lld:C0242350 a ncit:C7057 .
  
  dgn-gda:DGN9d9cfbd368ae76d86c90c4165e5e7f76 sio:SIO_000628 miriam-gene:63036, lld:C0242350;
    a sio:SIO_001122 .
}

dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_provenance {
  dgn-np:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_assertion dcterms:description
      "[To our knowledge, this is the first genome-wide association study to identify SNPs associated with adverse effects resulting from radiotherapy. It is important to note that the SNP that proved to be significantly associated with ED is located within a gene whose encoded product plays a role in male gonad development and function. Another key finding of this project is that the four SNPs most strongly associated with ED were specific to persons of African ancestry and would therefore not have been identified had a cohort of European ancestry been screened. This study demonstrates the feasibility of a genome-wide approach to investigate genetic predisposition to radiation injury.]. 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:20932654;
    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:NP95517.RADns9fhRp3L9yR6MRTZ1E2whMN__4Sq1CcpHW0jj9cfs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
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