@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0> .
@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:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_head {
  this: np:hasAssertion dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_assertion;
    np:hasProvenance dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_provenance;
    np:hasPublicationInfo dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_assertion a np:Assertion .
  
  dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_provenance a np:Provenance .
  
  dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_assertion {
  miriam-gene:196883 a ncit:C16612 .
  
  lld:C0007095 a ncit:C7057 .
  
  dgn-gda:DGNff14bab8685561476b0ce983ef6daa2a sio:SIO_000628 miriam-gene:196883, lld:C0007095;
    a sio:SIO_001121 .
}

dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_provenance {
  dgn-np:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_assertion dcterms:description
      "[DNA underrepresentations of 11q were the most frequent findings in TC (8 of 17) and AC (4 of 6), whereas these aberrations were rare in LCNEC (1 of 3) and SCLC (0 of 3).]. 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:9777940;
    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:NP882618.RAlltmEcEOsliFLYWpotKmzV2GtRrvqc_JLYwf9t3mNF0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
}