@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE> .
@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:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_head {
   this: np:hasAssertion dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_assertion ;
    np:hasProvenance dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_provenance ;
    np:hasPublicationInfo dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_assertion a np:Assertion .
  dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_provenance a np:Provenance .
  dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_assertion {
   miriam-gene:3075 a ncit:C16612 .
  lld:C0024437 a ncit:C7057 .
  dgn-gda:DGNf9eea14e3771ab03d58c4d03689dfd7c sio:SIO_000628 miriam-gene:3075 , lld:C0024437 ;
    a sio:SIO_001122 .
}
dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_provenance {
   dgn-np:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_assertion dcterms:description "[Y402H polymorphism which has been suggested to be a major risk factor of AMD in Caucasians was found to be only marginally associated with exudative AMD with low frequency, whereas three adjacent SNPs in the CFH gene were significantly associated with AMD in Koreans.]. 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:18223247 ;
    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:NP651950.RAF5R_3aepRF6Fd9EnJkb9MfFK42AIZfxiqFNXDe7lVuE130_publicationInfo {
   this: dcterms:created "2016-05-13T12:46:40+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" .
}