@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk> .
@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:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_head {
  this: np:hasAssertion dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_assertion;
    np:hasProvenance dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_provenance;
    np:hasPublicationInfo dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_assertion a np:Assertion .
  
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      np:PublicationInfo .
}

dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_provenance {
  dgn-np:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_assertion dcterms:description
      "[We examined the association between ALS risk and single nucleotide polymorphisms (SNPs) in the gene x-ray repair complementing defective repair in Chinese hamster cells 1 (XRCC1) utilizing data from a case-control study and 2 genome-wide association studies (the study of Irish Amyotrophic Lateral Sclerosis and the National Institute of Neurological Disorders and Stroke (NINDS) genome-wide study in Amyotrophic Lateral Sclerosis and Neurologically Normal Controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP812069.RAFyQpJ2BmSZS-f4oQiuaabQP9Ml7G-62h8WLfLnWdFGk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:18+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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