@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_head {
   this: np:hasAssertion dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_assertion ;
    np:hasProvenance dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_provenance ;
    np:hasPublicationInfo dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_provenance a np:Provenance .
  dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_assertion {
   miriam-gene:3717 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_provenance {
   dgn-np:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_assertion dcterms:description "[We evaluated the association between genetic variation in JAK1 (10 SNPs), JAK2 (9 SNPs), TYK2 (5 SNPs), suppressors of cytokine signaling (SOCS)1 (2 SNPs), SOCS2 (2 SNPs), STAT1 (16 SNPs), STAT2 (2 SNPs), STAT3 (6 SNPs), STAT4 (21 SNPs), STAT5A (2 SNPs), STAT5B (3 SNPs), STAT6 (4 SNPs) with risk of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-2016 ;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP942223.RA8v4theZq_aRYyNJkNRY2oONhgOunMoSxepB9WilzES0130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:52+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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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}