@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE> .
@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:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_head {
  this: np:hasAssertion dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_assertion;
    np:hasProvenance dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_provenance;
    np:hasPublicationInfo dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_assertion a np:Assertion .
  
  dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_provenance a np:Provenance .
  
  dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_assertion {
  miriam-gene:60675 a ncit:C16612 .
  
  lld:C0022735 a ncit:C7057 .
  
  dgn-gda:DGN48169afbbb11c92ca19d2d0aece84c4b sio:SIO_000628 miriam-gene:60675, lld:C0022735;
    a sio:SIO_001121 .
}

dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_provenance {
  dgn-np:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_assertion dcterms:description
      "[Indeed, the evidence from several naturally inactivating mutations in the PROK2 and PROKR2 genes in patients with Kallmann syndrome and normosmic hypogonadotropic hypogonadism also indicate the essential role of PROK2 in olfactory bulb morphogenesis and GnRH secretion in humans.]. 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:20502053;
    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:NP395043.RAojV13lpdYlOtTBEMpPWwWmQ7mwIF4zFrPRVjT0LAULE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:55+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" .
}