@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA> .
@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:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_head {
  this: np:hasAssertion dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_assertion;
    np:hasProvenance dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_provenance;
    np:hasPublicationInfo dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_assertion a np:Assertion .
  
  dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_provenance a np:Provenance .
  
  dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_assertion {
  miriam-gene:6120 a ncit:C16612 .
  
  lld:C1260959 a ncit:C7057 .
  
  dgn-gda:DGNeb076a59e27a582c4516e3e5cab56755 sio:SIO_000628 miriam-gene:6120, lld:C1260959;
    a sio:SIO_001121 .
}

dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_provenance {
  dgn-np:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_assertion dcterms:description
      "[The Fisher exact test, Cochran-Mantel-Haenszel statistics, and Mann-Whitney U test were used to assess the effect of each SNP with respect to the following phenotypic manifestations: age at diagnosis, gender, affected eye, study and fellow eye visual acuity at diagnosis and at last follow-up, study eye best acuity during follow-up, presence of large drusen and retinal pigment epithelium (RPE) hyperpigmentation in study and fellow eye, choroidal neovascularization (CNV) angiographic subtype (classic vs occult), CNV size, presence of wet AMD in fellow eye, presence of dry AMD in fellow eye, and smoking history.]. 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:19796758;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  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:NP397113.RA3sq2oIgObRVpjkCSGF7-yFuTWtAficjGC-L36ent9kA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:56+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" .
}