@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E> .
@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:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_head {
  this: np:hasAssertion dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_assertion ;
    np:hasProvenance dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_provenance ;
    np:hasPublicationInfo dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_assertion a np:Assertion .
  dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_provenance a np:Provenance .
  dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_assertion {
  miriam-gene:629 a ncit:C16612 .
  lld:C0242383 a ncit:C7057 .
  dgn-gda:DGN3e77cb8ed75d8abb9160a7d2badc2d78 sio:SIO_000628 miriam-gene:629 , lld:C0242383 ;
    a sio:SIO_001122 .
}
dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_provenance {
  dgn-np:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_assertion dcterms:description "[An age, gender and ethnicity matched case-control study was conducted to genotype the representative single neucleotide polymorphisms (SNPs) loci including rs1061170 and rs1410996 in CFH, rs641153 and rs4151667 in BF and rs11200638 in HTRA1 gene in 144 exudative AMD patients and 126 normal controls using PCR-RFLP and direct resequencing.]. 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:19187590 ;
    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:NP64011.RARIjgOec4Nk89OWC__09YyM9Zw0k0DNrS319Wad2KP4E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+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" .
}