@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk> .
@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:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_head {
  this: np:hasAssertion dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_assertion;
    np:hasProvenance dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_provenance;
    np:hasPublicationInfo dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_assertion a np:Assertion .
  
  dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_provenance a np:Provenance .
  
  dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_assertion {
  miriam-gene:4976 a ncit:C16612 .
  
  lld:C0338508 a ncit:C7057 .
  
  dgn-gda:DGN689f515f026b063634755241b5313597 sio:SIO_000628 miriam-gene:4976, lld:C0338508;
    a sio:SIO_001121 .
}

dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_provenance {
  dgn-np:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_assertion dcterms:description
      "[Ninety-eight SNPs were selected to tag the common genetic variation in nine genes, namely OPTN (optineurin), RDX (radixin), SNX16 (sorting nexin 16), OPA1 (optic atrophy 1), MFN1 (mitofusin 1), MFN2 (mitofusin 2), PARL (presenilin associated, rhomboid-like), SOD2 (superoxide dismutase 2, mitochondrial) and CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1).]. 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:19754948;
    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:NP763189.RARaaWTsG0f7351pQPmFL99QRvDF82PxbgEBydR7EwZtk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:31+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" .
}