@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA> .
@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:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_head {
  this: np:hasAssertion dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion;
    np:hasProvenance dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance;
    np:hasPublicationInfo dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion a np:Assertion .
  
  dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance a np:Provenance .
  
  dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion {
  miriam-gene:51364 a ncit:C16612 .
  
  lld:C0022679 a ncit:C7057 .
  
  dgn-gda:DGNefb6e69d9e1b41da769c0b46abc9da59 sio:SIO_000628 miriam-gene:51364, lld:C0022679;
    a sio:SIO_001121 .
}

dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_provenance {
  dgn-np:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_assertion dcterms:description
      "[Animal models support the association between ZMYND10 and human PCD, given that zmynd10 knockdown in zebrafish caused ciliary paralysis leading to cystic kidneys and otolith defects and that knockdown in Xenopus interfered with ciliogenesis.]. 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:23891469;
    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:NP768925.RA-ksVa_IaTRQMwcHpp86EOlFQJCiPUorzWfnggqhHhdA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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>,
      <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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}