@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw> .
@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:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_head {
  this: np:hasAssertion dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_assertion;
    np:hasProvenance dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_provenance;
    np:hasPublicationInfo dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_assertion a np:Assertion .
  
  dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_provenance a np:Provenance .
  
  dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN9f13e2e0102eb2759bf01e3d973ab567 sio:SIO_000628 miriam-gene:7422, lld:C0242383;
    a sio:SIO_001122 .
}

dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_provenance {
  dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_assertion dcterms:description
      "[The HTRA1-rs11200638 and CFH-rs1410996/-rs2274700 variants were associated with response to PDT in this study population. These variants may be used for genetic biomarkers to estimate visual outcomes and recurrences in the response to PDT with significant predictive power.]. 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:20678803;
    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:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}