@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c> .
@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/v3.0.0/void/> .
dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_head {
   this: np:hasAssertion dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_assertion ;
    np:hasProvenance dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_provenance ;
    np:hasPublicationInfo dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_assertion a np:Assertion .
  dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_provenance a np:Provenance .
  dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_assertion {
   miriam-gene:10877 a ncit:C16612 .
  lld:C0242383 a ncit:C7057 .
  dgn-gda:DGN7c49055f54a232178bbd8b3d7aa76fd8 sio:SIO_000628 miriam-gene:10877 , lld:C0242383 ;
    a sio:SIO_001121 .
}
dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_provenance {
   dgn-np:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_assertion dcterms:description "[Haplotype analysis supported our findings of single SNP association, demonstrating that the most significant haplotype, GATAGTTCTC, spanning CFH, CFHR4, and CFHR2 was associated with the greatest risk of developing neovascular AMD (P &lt; 10-6).]. 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:18541031 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP854752.RAswR63hnp56Ht1Q1AgkiWw8qzi4InrQ34MB81j3IKp6c130_publicationInfo {
   this: dcterms:created "2015-08-25T14:46:19+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}