@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928> .
@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:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_head {
  this: np:hasAssertion dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_assertion;
    np:hasProvenance dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_provenance;
    np:hasPublicationInfo dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_assertion a np:Assertion .
  
  dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_provenance a np:Provenance .
  
  dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_assertion {
  miriam-gene:5428 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGN4bf76f3d14c33ae0b7d7bf81c28af529 sio:SIO_000628 miriam-gene:5428, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_provenance {
  dgn-np:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_assertion dcterms:description
      "[To date over 40 disease mutations and 9 nonsynonymous polymorphisms in POLG have been found to be associated with autosomal recessive and dominant progressive external ophthalmoplegia (PEO), Alpers syndrome, sensory ataxia, neuropathy, dysarthria and ophthalmoparesis (SANDO), Parkinsonism, and male infertility.]. 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:15913923;
    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:NP200912.RAS_T1G7WnTo_kMRvRiCKnW1X67Nkq3d7b6bd3Ja5A928130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:51+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" .
}