@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU> .
@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:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_head {
  this: np:hasAssertion dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_assertion;
    np:hasProvenance dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_provenance;
    np:hasPublicationInfo dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_assertion a np:Assertion .
  
  dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_provenance a np:Provenance .
  
  dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGNd68548f7944b360c191f59065b50714e sio:SIO_000628 miriam-gene:5925, lld:C0035335;
    a sio:SIO_001122 .
}

dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_provenance {
  dgn-np:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_assertion dcterms:description
      "[Gene testing is indicated in the medical practice of hereditary retinoblastoma for familial risk assessment, while prior counseling is important for an understanding of the risks and benefits of gene testing. With improvements in patient prognosis, counseling for adult survivors is increasing in importance. Assessment of genetic risk to the offspring and prevention of secondary cancer are the primary issues of concern. Presymptomatic diagnosis of infants is effective for the proper assessment of the genetic risk and for making follow-up schedules for the detection of the tumor at an early stage.]. 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:15162822;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52363.RACS5_U9Cah_PLna_OOono1uUMukj_gF5hs26svoJvsqU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}