@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0> .
@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:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_head {
  this: np:hasAssertion dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_assertion;
    np:hasProvenance dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_provenance;
    np:hasPublicationInfo dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_assertion a np:Assertion .
  
  dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_provenance a np:Provenance .
  
  dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_assertion {
  miriam-gene:3552 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN8f7338d83510d142548d49b158c0119d sio:SIO_000628 miriam-gene:3552, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_provenance {
  dgn-np:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_assertion dcterms:description
      "[The 4-bp insertion/deletion (Indel) polymorphism (rs3783553) within the 3' untranslated regions of IL1A gene has been suggested to be associated with risk of various types of cancers, possibly through regulating expression of IL-1α levels.]. 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:23542780;
    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:NP379713.RAmYx8rX2ybbPi7PMyd98eIwnlHMg-tcgz0g3parW_GI0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:44+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" .
}