@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA> .
@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:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_head {
  this: np:hasAssertion dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_assertion;
    np:hasProvenance dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_provenance;
    np:hasPublicationInfo dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_assertion a np:Assertion .
  
  dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_provenance a np:Provenance .
  
  dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_assertion {
  miriam-gene:10252 a ncit:C16612 .
  
  lld:C1609433 a ncit:C7057 .
  
  dgn-gda:DGNb91ac65c20f761f2e345b6dab3f9751e sio:SIO_000628 miriam-gene:10252, lld:C1609433;
    a sio:SIO_001121 .
}

dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_provenance {
  dgn-np:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_assertion dcterms:description
      "[Individual or a combination of GDNF, RET and SPRY1 mutant alleles in mice cause renal malformations reminiscent of congenital anomalies of the kidney or urinary tract (CAKUT) in humans and distinct from renal agenesis phenotype in complete GDNF or RET-null mice.]. 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:22729463;
    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:NP273931.RAW9z3Ye8uLr_W5XdJ_M9dn1cmyEh0MULNCLljAWXzzMA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}