@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY> .
@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:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_head {
  this: np:hasAssertion dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion;
    np:hasProvenance dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance;
    np:hasPublicationInfo dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion a np:Assertion .
  
  dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance a np:Provenance .
  
  dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion {
  miriam-gene:3814 a ncit:C16612 .
  
  lld:C0342544 a ncit:C7057 .
  
  dgn-gda:DGN835135e089106be839b2265fe83e9526 sio:SIO_000628 miriam-gene:3814, lld:C0342544;
    a sio:SIO_001121 .
}

dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_provenance {
  dgn-np:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_assertion dcterms:description
      "[More recently, rare activating mutations of the kisspeptin and its receptor were identified in children with idiopathic central precocious puberty, supporting the crucial role of this system in the human pubertal onset.]. 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:20816945;
    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:NP242296.RACbLqihgCjdZwt3-Ya0re5evuLLNf1JBL-e2uu73duWY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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" .
}