@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk> .
@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:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_head {
  this: np:hasAssertion dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_assertion ;
    np:hasProvenance dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_provenance ;
    np:hasPublicationInfo dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_assertion a np:Assertion .
  dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_provenance a np:Provenance .
  dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_assertion {
  miriam-gene:27130 a ncit:C16612 .
  lld:C0687120 a ncit:C7057 .
  dgn-gda:DGNd71a4e9e840fcbe6ede2209859d7213e sio:SIO_000628 miriam-gene:27130 , lld:C0687120 ;
    a sio:SIO_001121 .
}
dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_provenance {
  dgn-np:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_assertion dcterms:description "[Cilia are comprised of distinct structural and functional subregions including the basal body, transition zone (TZ) and inversin (Inv) compartments, and defects in this organelle are associated with an expanding spectrum of inherited disorders including Bardet-Biedl syndrome (BBS), Meckel-Gruber Syndrome (MKS), Joubert Syndrome (JS) and Nephronophthisis (NPHP).]. 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:24339792 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP886250.RAbBMN8W12kcObsWIYmN6qJN-B-41IN50OnSig2jeLSLk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:40+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" .
}