@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP354523.RAJMdyya2EhZlGUjzes_vISiNmDwLrECJewuC__SkuOdM> .
@prefix sub: <http://rdf.disgenet.org/resource/nanopub/NP354523.RAJMdyya2EhZlGUjzes_vISiNmDwLrECJewuC__SkuOdM#> .
@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 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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v5.0.0/void/> .

sub:head {
  this: np:hasAssertion sub:assertion;
    np:hasProvenance sub:provenance;
    np:hasPublicationInfo sub:publicationInfo;
    a np:Nanopublication .
}

sub:assertion {
  dgn-gda:DGN7d8e03330797f53eb1702ab426b3589d sio:SIO_000628 miriam-gene:2068, lld:C0268138;
    a sio:SIO_001121 .
}

sub:provenance {
  sub:assertion dcterms:description "[Various combinations of the keywords and MeSH terms were used to screen for potentially relevant studies, specifically 'genetic polymorphisms' or 'SNPs' or 'variation' or 'single nucleotide polymorphism' or 'polymorphism' or 'mutation' or 'variant'; 'X-ray repair cross complementing protein 1' or 'Xeroderma Pigmentosum Group D Protein' or 'X-ray repair cross complementing protein 1' or 'Xeroderma Pigmentosum Group D Protein' or 'XPD' or 'Xeroderma Pigmentosum Complementation Group D Protein' or 'ERCC2' or 'XRCC1' or 'XRCC1 DNA repair protein'; and 'Cataract' or ' Membranous Cataract' or ' Pseudoaphakia.]. 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:25873778;
    prov:wasDerivedFrom dgn-void:BEFREE;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:BEFREE pav:importedOn "2017-02-19"^^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 .
}

sub:publicationInfo {
  this: dcterms:created "2017-10-17T13:12:26+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:disgenetv3.0rdf;
    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 "v5.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v5.0.0" .
}