@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI> .
@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:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_head {
  this: np:hasAssertion dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion;
    np:hasProvenance dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance;
    np:hasPublicationInfo dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion a np:Assertion .
  
  dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance a np:Provenance .
  
  dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion {
  miriam-gene:2334 a ncit:C16612 .
  
  lld:C2752082 a ncit:C7057 .
  
  dgn-gda:DGNba6b5dd61b3e538c5f4ec3366228db4c sio:SIO_000628 miriam-gene:2334, lld:C2752082;
    a sio:SIO_001121 .
}

dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_provenance {
  dgn-np:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_assertion dcterms:description
      "[Since these activities likely extend to the entire ALF protein family, this study also significantly inputs our understanding of the molecular basis of FRAXE mental retardation syndrome in which FMR2 expression is silenced.]. 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:17135274;
    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:NP737074.RAfXNm-CWeqE5LvFZegdK_qkMkiIMEw99Lqrb9wYwaURI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:27+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" .
}