@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks> .
@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:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_head {
   this: np:hasAssertion dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_assertion ;
    np:hasProvenance dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_provenance ;
    np:hasPublicationInfo dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_assertion a np:Assertion .
  dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_provenance a np:Provenance .
  dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_assertion {
   miriam-gene:2668 a ncit:C16612 .
  lld:C0000768 a ncit:C7057 .
  dgn-gda:DGNfa2c0860aaf90692febda0396f282ea8 sio:SIO_000628 miriam-gene:2668 , lld:C0000768 ;
    a sio:SIO_001121 .
}
dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_provenance {
   dgn-np:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_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-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:NP422269.RAl4Oew3cRM87VevAXN87TDl6FeZxJ9xonmQCHesem1Ks130_publicationInfo {
   this: dcterms:created "2015-08-25T14:41:46+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" .
}