@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY> .
@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 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:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_head {
  this: np:hasAssertion dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion;
    np:hasProvenance dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance;
    np:hasPublicationInfo dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion a np:Assertion .
  
  dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance a np:Provenance .
  
  dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C0007570 a ncit:C7057 .
  
  dgn-gda:DGNe2662c227dfaa178dfa2165c63e4d70e sio:SIO_000628 miriam-gene:3553, lld:C0007570;
    a sio:SIO_001122 .
}

dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_provenance {
  dgn-np:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_assertion dcterms:description
      "[The association between IL-10 genotypes and both histological severity at diagnosis and age of onset could be related to an alteration in cytokine balance, and supports the idea that the various clinical manifestations of the disease could be determined by a different genetic background.]. 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:16540751;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP56342.RA2upUYD1UToMPiEJEO50qj0n83Wo5OnqJpxjIZNW_OAY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}