@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM> .
@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:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_head {
  this: np:hasAssertion dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_assertion;
    np:hasProvenance dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_provenance;
    np:hasPublicationInfo dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_assertion a np:Assertion .
  
  dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_provenance a np:Provenance .
  
  dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_assertion {
  miriam-gene:3080 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN75746f983d9795fce79e7d1fd3911469 sio:SIO_000628 miriam-gene:3080, lld:C0242383;
    a sio:SIO_001122 .
}

dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_provenance {
  dgn-np:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_assertion dcterms:description
      "[Haplotype analysis supported our findings of single SNP association, demonstrating that the most significant haplotype, GATAGTTCTC, spanning CFH, CFHR4, and CFHR2 was associated with the greatest risk of developing neovascular AMD (P < 10-6).]. 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:18541031;
    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:NP67039.RAhxW3gAYSJ7EidKmwsH0H2L_aWdSQyZI7RzU04tWoEgM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}