@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558> .
@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:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_head {
  this: np:hasAssertion dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_assertion;
    np:hasProvenance dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_provenance;
    np:hasPublicationInfo dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_assertion a np:Assertion .
  
  dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_provenance a np:Provenance .
  
  dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_assertion {
  miriam-gene:966 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGNf86fbb116825c54dd380986a3437d342 sio:SIO_000628 miriam-gene:966, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_provenance {
  dgn-np:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_assertion dcterms:description
      "[In maculae of AMD specimens, we found that the complement regulatory protein, CD59, was increased in regions of uninvolved retinal pigmented epithelium (RPE) of early AMD, but decreased in the RPE overlying drusen and in geographic atrophy, an advanced form of AMD.]. 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:23097248;
    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:NP164011.RA83OohMjgiUKBOkTmx1m8qVPHMytIgC09MWsGN6Rc558130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}