@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs> .
@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:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_head {
  this: np:hasAssertion dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_assertion ;
    np:hasProvenance dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_provenance ;
    np:hasPublicationInfo dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_assertion a np:Assertion .
  dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_provenance a np:Provenance .
  dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_assertion {
  miriam-gene:3479 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN70f3c879d41230432901a2ecce02ac7d sio:SIO_000628 miriam-gene:3479 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_provenance {
  dgn-np:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_assertion dcterms:description "[A CA repeat polymorphism, in the IGF1 gene, which is located 969 bp upstream from the transcription start site and the rs2854744 and rs2854746 single nucleotide polymorphisms (SNPs) in the IGFBP3 gene have been associated with the serum levels of the respective proteins and colorectal cancer (CRC), but the results are inconsistent.]. 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:18031946 ;
    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:NP250033.RAWK_HuRR0ms3hgu4pEjzz40JCBoqfiOOfZGn7J2LUuYs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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> ;
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}