@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ> .
@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:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_head {
  this: np:hasAssertion dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_assertion;
    np:hasProvenance dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_provenance;
    np:hasPublicationInfo dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_assertion a np:Assertion .
  
  dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_provenance a np:Provenance .
  
  dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_assertion {
  miriam-gene:5122 a ncit:C16612 .
  
  lld:C0085413 a ncit:C7057 .
  
  dgn-gda:DGN381a2f66b124ab0f3db6404d60b26871 sio:SIO_000628 miriam-gene:5122, lld:C0085413;
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}

dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_provenance {
  dgn-np:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_assertion dcterms:description
      "[We show that confluent primary ADPKD cyst cells with the novel PC1 mutation DeltaL2433 and with normal abundance of PC1 and PC2 polypeptides lack ciliary PC1 and often lack ciliary PC2, whereas PC1 and PC2 are both present in cilia of confluent normal human kidney (NK) epithelial cells in primary culture.]. 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:17090781;
    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:NP670208.RAppcVeG92n6leL98SJZDpyqeG5PQDItSZj06LCkX0mNQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:44+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}