@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4> .
@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:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_head {
  this: np:hasAssertion dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_assertion;
    np:hasProvenance dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_provenance;
    np:hasPublicationInfo dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_assertion a np:Assertion .
  
  dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_provenance a np:Provenance .
  
  dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_assertion {
  miriam-gene:6741 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGN301a39a6220f2684fe062c6f02fa0eca sio:SIO_000628 miriam-gene:6741, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_provenance {
  dgn-np:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_assertion dcterms:description
      "[To show the functionality of the 280His variant, we evaluated single-strand break (SSB) repair capacity of isogenic Chinese hamster ovary cells expressing human forms of XRCC1 after exposure to hydrogen peroxide (H(2)O(2)), methyl methanesulfonate (MMS), or camptothecin by monitoring NAD(P)H. We used data from the Carolina Breast Cancer Study (CBCS), a population-based, case-control study that included 2,077 cases (786 African Americans and 1,281 Whites) and 1,818 controls (681 African Americans and 1,137 Whites), to examine associations among XRCC1 codon 194, 280, and 399 genotypes, breast cancer, and smoking.]. 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:16510609;
    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:NP673832.RA29tFwx5-qRACH3U3vyOFMmrNsBWUalt78v8pNueSjv4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:47+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" .
}