@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA> .
@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:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_head {
  this: np:hasAssertion dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_assertion ;
    np:hasProvenance dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_provenance ;
    np:hasPublicationInfo dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_assertion a np:Assertion .
  dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_provenance a np:Provenance .
  dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  lld:C0010346 a ncit:C7057 .
  dgn-gda:DGN0bdf4ca81de04cda33b9e4fa914bf00f sio:SIO_000628 miriam-gene:64127 , lld:C0010346 ;
    a sio:SIO_001122 .
}
dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_provenance {
  dgn-np:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_assertion dcterms:description "[From the CARD15 gene mutations in the adult Crohn's disease population the 1007finsC, while in the pediatric population the 1007finsC and the G908R were significantly associated with an increased risk for Crohn's disease.]. 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:19103559 ;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP244614.RAivUFzHlpdiU71l6gon-A3PO2FcY0ZLP8uX734hkEmtA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:37+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" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}