@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE> .
@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/v4.0.0/void/> .

dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_head {
  this: np:hasAssertion dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_assertion;
    np:hasProvenance dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_provenance;
    np:hasPublicationInfo dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_assertion a np:Assertion .
  
  dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_provenance a np:Provenance .
  
  dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN409cb931676f584c4686de0db9f898fa sio:SIO_000628 miriam-gene:3075, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_provenance {
  dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_assertion dcterms:description
      "[In addition to the higher risk for exudative AMD in patients with the CFH 402HH genotype that was found in previous studies, our results show that the CFH 402HH genotype also correlates with lower visual acuity outcome after treatment with bevacizumab, suggesting that pharmacogenetics of CFH plays a role in response to treatment of wet AMD.]. 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:21232084;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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 .
}

dgn-np:NP865136.RAEX0EEPRAFnIMafgl_TsqQcptm2HiFeM-OSg9ByxsQgE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:17+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}