@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM> .
@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/> .
@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-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_head {
  this: np:hasAssertion dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_assertion;
    np:hasProvenance dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_provenance;
    np:hasPublicationInfo dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_assertion a np:Assertion .
  
  dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_provenance a np:Provenance .
  
  dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C1720452 a ncit:C7057 .
  
  dgn-gda:DGNa5ed2a374c7fdb0686c9c27e761bc27a sio:SIO_000628 miriam-gene:3075, lld:C1720452;
    a sio:SIO_001122 .
}

dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_provenance {
  dgn-np:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_assertion dcterms:description
      "[After adjusting for age and other covariants, the CFH CC (Y402H polymorphism) genotype was associated with an increased likelihood of bilateral compared with unilateral involvement by any soft drusen (odds ratio [OR], 2.5; 95% confidence interval [CI], 1.4-4.5), distinct soft drusen (OR, 2.8; 95% CI, 1.0-8.1), and pigmentary abnormalities (OR, 1.7; 95% CI, 1.0-2.8).]. 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:19822851;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP446593.RAth5c7TAwmu8Bb_a1tfHRTkLYQXfgDXk0jG2pVS0MbRM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:01+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}