@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c> .
@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:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_head {
  this: np:hasAssertion dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_assertion ;
    np:hasProvenance dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_provenance ;
    np:hasPublicationInfo dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_assertion a np:Assertion .
  dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_provenance a np:Provenance .
  dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_assertion {
  miriam-gene:4650 a ncit:C16612 .
  lld:C0009324 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_provenance {
  dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_assertion dcterms:description "[To investigate the contribution of three polymorphisms of MYO9B gene for predisposition to Crohn's disease and ulcerative colitis, their association with clinical phenotypes, particularly intestinal permeability, and possible interaction with the CARD15 gene.]. 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:17944996 ;
    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 ;
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}
dgn-np:NP436498.RA0p4F3jjkKhDkBcYuQeR1-q4nTnxZcYTi6ql4zoL0X2c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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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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}