@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs> .
@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:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_head {
  this: np:hasAssertion dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion;
    np:hasProvenance dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance;
    np:hasPublicationInfo dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion a np:Assertion .
  
  dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance a np:Provenance .
  
  dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion {
  miriam-gene:3973 a ncit:C16612 .
  
  lld:C0851265 a ncit:C7057 .
  
  dgn-gda:DGN123d661f70eed48ef7b1a7236798cd61 sio:SIO_000628 miriam-gene:3973, lld:C0851265;
    a sio:SIO_001121 .
}

dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_provenance {
  dgn-np:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_assertion dcterms:description
      "[Chronic manifestations, which also develop in prospectively treated patients, involve (a) the brain, resulting in delayed language acquisition, speech defects, and learning problems, and (b) the ovary, in the majority of females, producing hypergonadotropic hypogonadism.]. 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:18574215;
    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:NP213330.RAekYWduZsC3OVB0UwbCOPQ88XdIBxXQofXMz_VGn06Bs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}