@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0> .
@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:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_head {
  this: np:hasAssertion dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_assertion;
    np:hasProvenance dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_provenance;
    np:hasPublicationInfo dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_assertion a np:Assertion .
  
  dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_provenance a np:Provenance .
  
  dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_assertion {
  miriam-gene:2098 a ncit:C16612 .
  
  lld:C0751483 a ncit:C7057 .
  
  dgn-gda:DGNad8517c07124f353b794b0f728e6289c sio:SIO_000628 miriam-gene:2098, lld:C0751483;
    a sio:SIO_001121 .
}

dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_provenance {
  dgn-np:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_assertion dcterms:description
      "[Evaluation of three families with hereditary retinoblastoma demonstrates close linkage of the gene for this tumor with the genetic locus for esterase D. These results assign the gene for the hereditary form of retinoblastoma to band q14 on chromosome 13, the same region which is affected in the chromosome deletion form of this eye tumor, and therefore suggest a common underlying mechanism in the pathogenesis of these two forms of retinoblastoma.]. 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:6823558;
    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:NP451437.RAHTB2iSv1UmPL0KvLc4yre1r2FEyWnjHFeNy00a2Lwb0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}