@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA> .
@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:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_head {
  this: np:hasAssertion dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_assertion;
    np:hasProvenance dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_provenance;
    np:hasPublicationInfo dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_assertion a np:Assertion .
  
  dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_provenance a np:Provenance .
  
  dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_assertion {
  miriam-gene:2078 a ncit:C16612 .
  
  lld:C0750957 a ncit:C7057 .
  
  dgn-gda:DGN4e1353007ca5b7cdf8d22d2027718881 sio:SIO_000628 miriam-gene:2078, lld:C0750957;
    a sio:SIO_001121 .
}

dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_provenance {
  dgn-np:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_assertion dcterms:description
      "[This autosomal recessive condition is usually recognized at birth or during the first months of life in an infant with total blindness or greatly impaired vision, normal fundus and extinguished electroretinogram (ERG).]. 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:8944027;
    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:NP787530.RAuPdZRAq_PZIAT8z_SmymjXn_tD0DXHwP5MJhw4fltpA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}