@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row> .
@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:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_head {
  this: np:hasAssertion dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_assertion;
    np:hasProvenance dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_provenance;
    np:hasPublicationInfo dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_assertion a np:Assertion .
  
  dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_provenance a np:Provenance .
  
  dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_assertion {
  miriam-gene:7916 a ncit:C16612 .
  
  lld:C0009324 a ncit:C7057 .
  
  dgn-gda:DGNbb9385d45dcfdfbddc2ece8ae99f4e63 sio:SIO_000628 miriam-gene:7916, lld:C0009324;
    a sio:SIO_001122 .
}

dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_provenance {
  dgn-np:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_assertion dct:description
      "[ The above-mentioned pattern, most likely formed by recombination of the telomeric fragment of the MHC 7.1 ancestral haplotype, seems to be the most important genetic determinant of susceptibility to the extensive form of UC in our population.]. 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:16116311;
    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:NP47893.RAg9Ngk79R2cs1inczURWTG8AQCJwWSEbNaIIXCWn6row130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct: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" .
}