@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s> .
@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/v3.0.0/void/> .

dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_head {
  this: np:hasAssertion dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_assertion;
    np:hasProvenance dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_provenance;
    np:hasPublicationInfo dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_assertion a np:Assertion .
  
  dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_provenance a np:Provenance .
  
  dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_assertion {
  miriam-gene:5015 a ncit:C16612 .
  
  lld:C0035334 a ncit:C7057 .
  
  dgn-gda:DGN4c98488d15bd5f9753e4d405226d98ff sio:SIO_000628 miriam-gene:5015, lld:C0035334;
    a sio:SIO_001121 .
}

dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_provenance {
  dgn-np:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_assertion dcterms:description
      "[The expression pattern of OTX2 in human embryos is consistent with the eye phenotypes observed in the patients, which range from bilateral anophthalmia to retinal defects resembling Leber congenital amaurosis and pigmentary retinopathy.]. 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:15846561;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP604233.RABm-IeJLrvYDGVGH8Fa2RFIVhsTcpvcNqyB2-RjNa-4s130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:41+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}