@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_head {
  this: np:hasAssertion dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_assertion;
    np:hasProvenance dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_provenance;
    np:hasPublicationInfo dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_assertion a np:Assertion .
  
  dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_provenance a np:Provenance .
  
  dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_assertion {
  miriam-gene:2334 a ncit:C16612 .
  
  lld:C0006009 a ncit:C7057 .
  
  dgn-gda:DGNb3387a0b2f31a0bef9041395370eee6b sio:SIO_000628 miriam-gene:2334, lld:C0006009;
    a sio:SIO_001121 .
}

dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_provenance {
  dgn-np:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_assertion dcterms:description
      "[Although the role of FMR3 in FRAXE associated mild to borderline mental retardation is not yet clear, lack of expression of FMR3 in FRAXE full mutation males means that the FMR3 gene is potentially involved.]. 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:11015457;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP296561.RALMllgPd0j3tSHJGDpIYMnNYzeMUlMitXGEWeD5r0L3A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:00+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}