@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY> .
@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:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_head {
   this: np:hasAssertion dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_assertion ;
    np:hasProvenance dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_provenance ;
    np:hasPublicationInfo dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_assertion a np:Assertion .
  dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_provenance a np:Provenance .
  dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_assertion {
   miriam-gene:84680 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN058693a61817f97a81c6a0006bf826bd sio:SIO_000628 miriam-gene:84680 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_provenance {
   dgn-np:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_assertion dcterms:description "[In order to determine whether adenoma-carcinoma sequence (ACS) or de novo cancer development, generally considered to be two separate genetic pathways, might be responsible, K-ras codon 12 mutations, good markers for ACS, were examined in 59 and 84 cases of advanced colorectal cancer surgically resected in Cancer Institute Hospital of the Japanese Foundation for Cancer Research in 1960-1969 and in 1990-1999, respectively.]. 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:15819719 ;
    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:NP211024.RAbei8M25315An24xIHJJbfeNwKj3KPqjmPuHGZmjdIGY130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:56+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" .
}