@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI> .
@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:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_head {
  this: np:hasAssertion dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion;
    np:hasProvenance dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance;
    np:hasPublicationInfo dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion a np:Assertion .
  
  dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance a np:Provenance .
  
  dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion {
  miriam-gene:5551 a ncit:C16612 .
  
  lld:C0149925 a ncit:C7057 .
  
  dgn-gda:DGNbd3db3e9c3b07dcd3218d70532ce9187 sio:SIO_000628 miriam-gene:5551, lld:C0149925;
    a sio:SIO_001121 .
}

dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_provenance {
  dgn-np:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_assertion dcterms:description
      "[From this starting point, a P1 contig was developed for the region of 450 Kb that is common to the homozygous deletions seen in the SCLC lines NCI H740 and GLC20 and is also present in HA(3)BB9F, the suppressed A9 hybrid.]. 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:8957080;
    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:NP640063.RA83FcgFz8-t9IJflx1s4CJ3BvFkX0rXl4Avfmq6zpfTI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:03+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" .
}