@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw> .
@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:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_head {
  this: np:hasAssertion dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_assertion;
    np:hasProvenance dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_provenance;
    np:hasPublicationInfo dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_assertion a np:Assertion .
  
  dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_provenance a np:Provenance .
  
  dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_assertion {
  miriam-gene:9501 a ncit:C16612 .
  
  lld:C0025149 a ncit:C7057 .
  
  dgn-gda:DGN3c566d5f6493fd1d4e558fad79a96f24 sio:SIO_000628 miriam-gene:9501, lld:C0025149;
    a sio:SIO_001121 .
}

dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_provenance {
  dgn-np:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_assertion dcterms:description
      "[We determined the exon-intron boundaries of RPH3AL and screened the coding region for mutations by direct sequencing in DNA extracted from 33 tumor samples with allelic loss of 17p13, including 10 medulloblastoma, 14 follicular thyroid cancer (FTC), and 9 ovarian cancer specimens.]. 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:10395805;
    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:NP586956.RA_ZkFzkiIP4gqbmlMfvf49amjVfOtqdsHul8HfbUlZBw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:53+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" .
}