@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA> .
@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:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_head {
  this: np:hasAssertion dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_assertion;
    np:hasProvenance dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_provenance;
    np:hasPublicationInfo dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_assertion a np:Assertion .
  
  dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_provenance a np:Provenance .
  
  dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0016053 a ncit:C7057 .
  
  dgn-gda:DGNeae1499082aa5bfd2cb717a2bec79b6e sio:SIO_000628 miriam-gene:2332, lld:C0016053;
    a sio:SIO_001121 .
}

dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_provenance {
  dgn-np:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_assertion dcterms:description
      "[The early detection of premutation carriers for the FMR1 gene among individuals diagnosed with fibromyalgia is important and would be helpful in correct genetic counseling of patients and their families, who may be at risk of having children with fragile X syndrome, the most common known cause of inherited intellectual disability and autism.]. 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:22903700;
    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:NP626727.RAtgXURjqSqD_3SM_17GKJMmEf-U79nq62OFxpZweXrfA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:18+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" .
}