@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM> .
@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:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_head {
  this: np:hasAssertion dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_assertion ;
    np:hasProvenance dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_provenance ;
    np:hasPublicationInfo dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_assertion a np:Assertion .
  dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_provenance a np:Provenance .
  dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0032227 a ncit:C7057 .
  dgn-gda:DGN9d3b84673c546983fa798857b3be7483 sio:SIO_000628 miriam-gene:7157 , lld:C0032227 ;
    a sio:SIO_001121 .
}
dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_provenance {
  dgn-np:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_assertion dcterms:description "[To determine whether the genetic analysis of pleural fluid can be used to diagnose malignant effusion, we investigated p53 and FHIT mutations and microsatellite alterations (MA) in the pleural fluid of 40 patients with pleural effusion associated with malignancy (ME) and in the pleural fluid of 17 patients with tuberculous pleurisy (TB) as a control group.]. 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:15013581 ;
    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:NP221604.RANwmmHziJKp3vPX_Jnc1flx3WTHYyMIKF9ZSujFowLNM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:03+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: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" .
}