@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo> .
@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:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_head {
  this: np:hasAssertion dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion;
    np:hasProvenance dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance;
    np:hasPublicationInfo dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion a np:Assertion .
  
  dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance a np:Provenance .
  
  dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion {
  miriam-gene:7864 a ncit:C16612 .
  
  lld:C0001418 a ncit:C7057 .
  
  dgn-gda:DGN586d16997197887e1ec23634e69a6540 sio:SIO_000628 miriam-gene:7864, lld:C0001418;
    a sio:SIO_001121 .
}

dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_provenance {
  dgn-np:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_assertion dcterms:description
      "[The frequency of detection of the A1/A1 genotype in the tumor tissues was increased in adenocarcinoma patients as compared with the blood of adenocarcinoma patients and was decreased in the blood of SCLC patients as compared with the blood of healthy individuals.]. 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:8608979;
    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:NP373142.RA19mHCLQ3RVaPdPhiQtgud8mBKNX4OKbBzvSnoMxBtlo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}