@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0> .
@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/v3.0.0/void/> .
dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_head {
  this: np:hasAssertion dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_assertion ;
    np:hasProvenance dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_provenance ;
    np:hasPublicationInfo dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_assertion a np:Assertion .
  dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_provenance a np:Provenance .
  dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0008313 a ncit:C7057 .
  dgn-gda:DGN72d3a5b63941f39e4fcd373f55ec2871 sio:SIO_000628 miriam-gene:1080 , lld:C0008313 ;
    a sio:SIO_001122 .
}
dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_provenance {
  dgn-np:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_assertion dcterms:description "[These data indicate that there is an increased prevalence of CFTR abnormalities in PSC as demonstrated by molecular and functional analyses and that these abnormalities may contribute to the development of PSC in a subset of patients with inflammatory bowel 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:12783301 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP56554.RA16oqQXLRkzfMOEQWlieL-XkEZBdVe93VImJE03kNsU0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:11+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}