@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8> .
@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:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_head {
  this: np:hasAssertion dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion ;
    np:hasProvenance dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance ;
    np:hasPublicationInfo dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion a np:Assertion .
  dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance a np:Provenance .
  dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion {
  miriam-gene:57332 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN94d52eac67acae7a953853cb7f083758 sio:SIO_000628 miriam-gene:57332 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_provenance {
  dgn-np:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_assertion dcterms:description "[N- and K-ras mutations at codons 12 and 13 were investigated using oligonucleotide hybridization analysis after PCR amplification and subsequent sequence analysis of the amplified DNA from the region of interest in the following prostatic primary and metastatic (met) carcinoma-derived cell lines: 1013L (primary), PC3 (bone met), DU145 (brain met), and LNCaP (lymph node met).]. 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:7678540 ;
    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:NP596041.RARGaCnV_HZcbk0h7FqoAm_Q7mV3an_awliliX53qw6E8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:58+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" .
}