@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms> .
@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:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_head {
  this: np:hasAssertion dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_assertion ;
    np:hasProvenance dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_provenance ;
    np:hasPublicationInfo dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_assertion a np:Assertion .
  dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_provenance a np:Provenance .
  dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  lld:C0011849 a ncit:C7057 .
  dgn-gda:DGNbec6302c3ca5a650fb53a5502d51fa5d sio:SIO_000628 miriam-gene:64127 , lld:C0011849 ;
    a sio:SIO_001121 .
}
dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_provenance {
  dgn-np:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_assertion dcterms:description "[The effect of rs2903692 previously described in diabetes was observed specifically for Crohn's disease (CD) patients lacking the main susceptibility factor described to date, that is, three polymorphisms within another pattern recognition gene, NOD2/CARD15 (NOD2(-) vs NOD2(+) CD patients, G vs A: P=0.008; OR (95% CI)=1.54 (1.10-2.15); NOD2(-) CD patients vs controls: P=0.008; OR (95% CI)=1.37 (1.08-1.73)).]. 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:19337309 ;
    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:NP400777.RA-dhmKpyF9fmKu8GJN7fZLkihmZ4_fwQmC61BLHznCms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:58+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" .
}