@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc> .
@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:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_head {
  this: np:hasAssertion dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion;
    np:hasProvenance dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance;
    np:hasPublicationInfo dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion a np:Assertion .
  
  dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance a np:Provenance .
  
  dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion {
  miriam-gene:2481 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGNda894fec20d2c759a6f122cfc73b605a sio:SIO_000628 miriam-gene:2481, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_provenance {
  dgn-np:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_assertion dcterms:description
      "[In contrast, a relationship between the second main group of fragile sites characterized by repeat expansion, the rare fragile sites, and mental retardation has been proposed many years ago, but after the molecular cloning of FRAXA and FRAXE both unequivocally involved in mental retardation, no additional fragile sites linked with mental retardation have been cloned for over a decade.]. 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:17567780;
    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:NP351214.RA1PHFzbVu2mswoqZ6weiThJKAnGSQnxY0RUi5x37t2rc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:26+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" .
}