@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g> .
@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:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_head {
  this: np:hasAssertion dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_assertion;
    np:hasProvenance dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_provenance;
    np:hasPublicationInfo dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_assertion a np:Assertion .
  
  dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_provenance a np:Provenance .
  
  dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN3bbd6daf95b810c4198e589e29d1f1b5 sio:SIO_000628 miriam-gene:3075, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_provenance {
  dgn-np:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_assertion dcterms:description
      "[The genotypes of the polymorphisms in the known AMD susceptibility loci (CFH, AMRS2, HTRA1, VEGFA, and KDR) were determined, and association between their frequencies and the changes in the BCVA and the CSMT were evaluated.]. 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:23559864;
    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:NP1066789.RAnde6x31UDbOe0cGycXHD1_b2v9FuKW33ddbQ3bGmx5g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:50+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" .
}