@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY> .
@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:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_head {
  this: np:hasAssertion dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_assertion;
    np:hasProvenance dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_provenance;
    np:hasPublicationInfo dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_assertion a np:Assertion .
  
  dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_provenance a np:Provenance .
  
  dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN69753c22d4469205b8e8402ce701e4e0 sio:SIO_000628 miriam-gene:2332, lld:C0004352;
    a sio:SIO_001121 .
}

dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_provenance {
  dgn-np:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_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:NP307457.RAdMcoI86EtRUfe_gFpjVtyXxdqfs5ulswhNQ5rROhDjY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:56+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" .
}