@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0> .
@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:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_head {
  this: np:hasAssertion dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_assertion;
    np:hasProvenance dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_provenance;
    np:hasPublicationInfo dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_assertion a np:Assertion .
  
  dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_provenance a np:Provenance .
  
  dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_assertion {
  miriam-gene:7507 a ncit:C16612 .
  
  lld:C0033999 a ncit:C7057 .
  
  dgn-gda:DGN59ef76dc561314c2e46f17b7f4544f09 sio:SIO_000628 miriam-gene:7507, lld:C0033999;
    a sio:SIO_001122 .
}

dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_provenance {
  dgn-np:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_assertion dcterms:description
      "[The XRCC1 codon 194 polymorphism causes a decreased risk of developing pterygium, but the codon 399 polymorphism increases the risk. There is no correlation between pterygium and XRCC1 codon 107 and 280, XPA A23G, and XPD codon 751 polymorphisms.]. 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:20431719;
    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:NP91438.RA3mBIPEf3cfktIyqv3NTsFFoO7H6SgNkJZ-Lcfmjwvl0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}