@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4> .
@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:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_head {
  this: np:hasAssertion dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion;
    np:hasProvenance dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance;
    np:hasPublicationInfo dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion a np:Assertion .
  
  dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance a np:Provenance .
  
  dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion {
  miriam-gene:4650 a ncit:C16612 .
  
  lld:C0021390 a ncit:C7057 .
  
  dgn-gda:DGN24bb5d3f8ab652a0ded6b671b1fce822 sio:SIO_000628 miriam-gene:4650, lld:C0021390;
    a sio:SIO_001121 .
}

dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance {
  dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion dcterms:description
      "[To date, seven studies have provided evidence for an association between the gene encoding for myosin IXB (MYO9B) and celiac disease (CD), and inflammatory bowel diseases, including single nucleotide polymorphisms (SNPs) rs2305767, rs1457092, and rs2305764.]. 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:20303373;
    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:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:46+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" .
}