@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA> .
@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:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_head {
  this: np:hasAssertion dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion;
    np:hasProvenance dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance;
    np:hasPublicationInfo dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion a np:Assertion .
  
  dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance a np:Provenance .
  
  dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN1fa7eca816c399665abf3b22e8f46672 sio:SIO_000628 miriam-gene:3075, lld:C0242383;
    a sio:SIO_001122 .
}

dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance {
  dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion dcterms:description
      "[Our findings indicate that the CFH gene is involved in the onset of AMD, whereas both, the CFH and ARMS2 genes, and more weakly, the HtrA1 gene, appear to account for the advancement 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:19169232;
    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:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}