@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk> .
@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:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_head {
  this: np:hasAssertion dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_assertion ;
    np:hasProvenance dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_provenance ;
    np:hasPublicationInfo dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_assertion a np:Assertion .
  dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_provenance a np:Provenance .
  dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_assertion {
  miriam-gene:1630 a ncit:C16612 .
  lld:C0007131 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_provenance {
  dgn-np:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_assertion dcterms:description "[Since the DCC candidate tumor suppressor gene has been mapped in this region, mutation and expression of the DCC gene were examined in 46 lung cancer cell lines, consisting of 14 small cell lung carcinomas (SCLCs) and 32 non-small cell lung carcinomas (NSCLCs), to elucidate the pathogenetic significance of DCC alterations in human lung carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP205818.RAlF1fdi05WzffuEP-wg18DkZ6nh1QNqNeibmLOk_9wvk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:53+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}