@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I> .
@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:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_head {
  this: np:hasAssertion dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_assertion;
    np:hasProvenance dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_provenance;
    np:hasPublicationInfo dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_assertion a np:Assertion .
  
  dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_provenance a np:Provenance .
  
  dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0456909 a ncit:C7057 .
  
  dgn-gda:DGN37405329f3a3ea8ba79a92853dce7a41 sio:SIO_000628 miriam-gene:3075, lld:C0456909;
    a sio:SIO_001121 .
}

dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_provenance {
  dgn-np:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_assertion dcterms:description
      "[Our findings strongly suggest that monogenic inheritance of CFH variants can result in basal laminar drusen in young adults, and this can progress to maculopathy and severe vision loss later in life.]. 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:18252232;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP824194.RAQRDEfIzQP_nX8W4RTbeloJ2fP-8agBRJYMHgdpQpi3I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:24+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" .
}