@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U> .
@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:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_head {
  this: np:hasAssertion dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion;
    np:hasProvenance dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance;
    np:hasPublicationInfo dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion a np:Assertion .
  
  dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance a np:Provenance .
  
  dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion {
  miriam-gene:9968 a ncit:C16612 .
  
  lld:C0338508 a ncit:C7057 .
  
  dgn-gda:DGNdcacda6641b9fb1d484371d9c9e6e2a3 sio:SIO_000628 miriam-gene:9968, lld:C0338508;
    a sio:SIO_001121 .
}

dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance {
  dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion dcterms:description
      "[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. 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:11810296;
    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:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:21+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: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" .
}