@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c> .
@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:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_head {
   this: np:hasAssertion dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_assertion ;
    np:hasProvenance dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_provenance ;
    np:hasPublicationInfo dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_assertion a np:Assertion .
  dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_provenance a np:Provenance .
  dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_assertion {
   miriam-gene:3342 a ncit:C16612 .
  lld:C0007131 a ncit:C7057 .
  dgn-gda:DGN1dc4a57a1fff6cc926c083da19574601 sio:SIO_000628 miriam-gene:3342 , lld:C0007131 ;
    a sio:SIO_001121 .
}
dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_provenance {
   dgn-np:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_assertion dcterms:description "[The overall pattern of chromosomal changes detected by spectral karyotype (SKY) analysis of two cell lines of each major histological subtype of NSCLC, namely squamous cell carcinoma (SQCC) and adenocarcinoma (ADC), indicated a greater degree of chromosomal rearrangement, than was present or predicted by either comparative genomic hybridization (CGH) or G-banding analysis alone.]. 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:11369051 ;
    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:NP793560.RAev061OvB5TMqgLNSsL6IFLYqDiUM6eMn98kSFtZme9c130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:07+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" .
}