@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4> .
@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:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_head {
  this: np:hasAssertion dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_assertion;
    np:hasProvenance dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_provenance;
    np:hasPublicationInfo dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_assertion a np:Assertion .
  
  dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_provenance a np:Provenance .
  
  dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_assertion {
  miriam-gene:373159 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGN8c84ca2dd6d18fb2000b62755ef33655 sio:SIO_000628 miriam-gene:373159, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_provenance {
  dgn-np:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_assertion dcterms:description
      "[Although the RD was ascribed to the deletion of RP2, the ID was suggested to be accounted for by the loss of ZNF674, which mutations were independently reported to account for isolated XLID.]. 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:22126752;
    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:NP691600.RApm0OhDeg5lvIYEcM3vtLNrI_rT97LUOy5SW6GGD4tC4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}