@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss> .
@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 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:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_head {
  this: np:hasAssertion dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_assertion;
    np:hasProvenance dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_provenance;
    np:hasPublicationInfo dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_assertion a np:Assertion .
  
  dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_provenance a np:Provenance .
  
  dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_assertion {
  miriam-gene:2477 a ncit:C16612 .
  
  lld:C0016667 a ncit:C7057 .
  
  dgn-gda:DGNa6beaa7b69cd1a111710414e6dd0ea83 sio:SIO_000628 miriam-gene:2477, lld:C0016667;
    a sio:SIO_001122 .
}

dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_provenance {
  dgn-np:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_assertion dct:description
      "[We have recently standardized and tested the diagnostic potential of a rapid antibody test on blood smears, based on the presence of FMRP, the protein product of the FMR1 gene, in lymphocytes from normal individuals and the absence of FMRP in lymphocytes in patients with FXS.]. 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:15900569;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP60359.RAws68FqXsOrGKE-OrQGW9xORkgDXvGrlqZCACgn_1Fss130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}