@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ> .
@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/v4.0.0/void/> .

dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_head {
  this: np:hasAssertion dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_assertion;
    np:hasProvenance dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_provenance;
    np:hasPublicationInfo dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_assertion a np:Assertion .
  
  dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_provenance a np:Provenance .
  
  dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_assertion {
  miriam-gene:8101 a ncit:C16612 .
  
  lld:C0001815 a ncit:C7057 .
  
  dgn-gda:DGNabd2a159267639378510479df2ac82a1 sio:SIO_000628 miriam-gene:8101, lld:C0001815;
    a sio:SIO_001121 .
}

dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_provenance {
  dgn-np:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_assertion dcterms:description
      "[To identify a commonly deleted region of 13q14 in idiopathic myelofibrosis (IMF), we used fluorescence in situ hybridization analysis to test for deletion of the RB1 and BRCA2 genes, and the microsatellite loci D13S319 and D13S25, in a series of 25 patients.]. 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:11380400;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP319326.RAZlWXSsCzproWkbJIp9qVgoXfZylgUXpom7QaVoINKvQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:10+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}