@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo> .
@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:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_head {
  this: np:hasAssertion dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion;
    np:hasProvenance dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance;
    np:hasPublicationInfo dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion a np:Assertion .
  
  dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance a np:Provenance .
  
  dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion {
  miriam-gene:387715 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN0acafee43bbb765525170523b9bfc8f0 sio:SIO_000628 miriam-gene:387715, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance {
  dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion dcterms:description
      "[On the basis of this and other results it is tempting to speculate that the combined effect of variants in the CFH and LOC 387715 genes may contribute to the AMD phenotype in this family.]. 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:17285240;
    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:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:14+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" .
}