@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc> .
@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:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_head {
  this: np:hasAssertion dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_assertion;
    np:hasProvenance dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_provenance;
    np:hasPublicationInfo dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_assertion a np:Assertion .
  
  dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_provenance a np:Provenance .
  
  dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_assertion {
  miriam-gene:128674 a ncit:C16612 .
  
  lld:C0271623 a ncit:C7057 .
  
  dgn-gda:DGN0653e0a98d24e7262c158288b60ba87e sio:SIO_000628 miriam-gene:128674, lld:C0271623;
    a sio:SIO_001121 .
}

dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_provenance {
  dgn-np:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_assertion dcterms:description
      "[Our goal was to determine whether variants in the first intracellular loop (ICL1) of PROKR2 (R80C, R85C, and R85H) identified in patients with hypogonadotropic hypogonadism interfere with receptor function and to elucidate the mechanisms of these effects.]. 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:22745195;
    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:NP435604.RAFGxhMTZdCfzD0ZTl9ALSOx-KbeptSyl7QKDzWiu3hcc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:18+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" .
}