@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo> .
@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:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_head {
  this: np:hasAssertion dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_assertion ;
    np:hasProvenance dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_provenance ;
    np:hasPublicationInfo dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_assertion a np:Assertion .
  dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_provenance a np:Provenance .
  dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_assertion {
  miriam-gene:149233 a ncit:C16612 .
  lld:C0010346 a ncit:C7057 .
  dgn-gda:DGN678ce4b3c846042f3dc60b8631ecaaf2 sio:SIO_000628 miriam-gene:149233 , lld:C0010346 ;
    a sio:SIO_001121 .
}
dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_provenance {
  dgn-np:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_assertion dcterms:description "[The use of techniques such as whole genome association studies to perform broad, unbiased screening for the contributions of common genetic variations to complex disease has rapidly assisted in the identification of several novel susceptibility loci associated with pediatric-onset Crohn's disease such as IL23R and ATG16L1.]. 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:17600381 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  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:NP617713.RASgyok-zoY4V3AMdg0gz7qsT-LeHxMOqXAvkzTj2FPRo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:25+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
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}