@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM> .
@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:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_head {
  this: np:hasAssertion dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_assertion;
    np:hasProvenance dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_provenance;
    np:hasPublicationInfo dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_assertion a np:Assertion .
  
  dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_provenance a np:Provenance .
  
  dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0149782 a ncit:C7057 .
  
  dgn-gda:DGNfb46853f678c841b6e01465769d5828d sio:SIO_000628 miriam-gene:3342, lld:C0149782;
    a sio:SIO_001121 .
}

dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_provenance {
  dgn-np:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_assertion dcterms:description
      "[We have used the molecular cytogenetic techniques of multicolor fluorescence in situ hybridization (M-FISH) and comparative genomic hybridization (CGH) to analyze two established lung cancer cell lines (A549, H520), 80 primary lung adenocarcinoma samples and 80 squamous cell lung carcinoma samples in order to identify common chromosomal aberrations.]. 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:18848758;
    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:NP730841.RAPyg208X9zzAZ4e28O-cJ2NQkwsAPchz5TDooigLk_GM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:23+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" .
}