@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858> .
@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:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_head {
  this: np:hasAssertion dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_assertion;
    np:hasProvenance dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_provenance;
    np:hasPublicationInfo dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_assertion a np:Assertion .
  
  dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_provenance a np:Provenance .
  
  dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_assertion {
  miriam-gene:649 a ncit:C16612 .
  
  lld:C0311245 a ncit:C7057 .
  
  dgn-gda:DGN8f9198b16f4d614db23ebb4e86fd83e9 sio:SIO_000628 miriam-gene:649, lld:C0311245;
    a sio:SIO_001121 .
}

dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_provenance {
  dgn-np:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_assertion dcterms:description
      "[Exciting data implicate PCP in normal kidney development and suggest the loss of oriented cell division and convergent extension downstream of defective PCP signaling lead to cystic kidney disease in mouse models.]. 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:19762494;
    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:NP837036.RAHkzgtwdCM_tFSaLOL0de8qVx4UM8KTeQio6sly1j858130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:32+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" .
}