@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM> .
@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:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_head {
  this: np:hasAssertion dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_assertion;
    np:hasProvenance dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_provenance;
    np:hasPublicationInfo dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_assertion a np:Assertion .
  
  dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_provenance a np:Provenance .
  
  dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_assertion {
  miriam-gene:29974 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_provenance {
  dgn-np:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_assertion dcterms:description
      "[These dysplastic ACF are, therefore, strongly considered to be putative preneoplastic lesions of the colon.A genetic trait affecting the susceptibility to colon carcinogenesis in F344 rats was mapped to chromosome 16, between D16Rat17 and D16Wox3, using the number of ACF as a surrogate biomarker for colon carcinogenesis.]. 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:12351153;
    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:NP664151.RAdpaHAGqkXNd0wp8NaNpyooGFtJKMbVHbibwrSTbvPtM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}