@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs> .
@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/v3.0.0/void/> .

dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_head {
  this: np:hasAssertion dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_assertion;
    np:hasProvenance dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_provenance;
    np:hasPublicationInfo dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_assertion a np:Assertion .
  
  dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_provenance a np:Provenance .
  
  dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_assertion {
  miriam-gene:2481 a ncit:C16612 .
  
  lld:C0242354 a ncit:C7057 .
  
  dgn-gda:DGN5e5cdb532fe4040904e72d54ded17fc9 sio:SIO_000628 miriam-gene:2481, lld:C0242354;
    a sio:SIO_001121 .
}

dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_provenance {
  dgn-np:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_assertion dcterms:description
      "[In dealing with patients who are found to have fragile sites, other than FRAXA, FRAXE and possibly FRA11B, considerable reassurance can be given that they are not at increased risk of having children with congenital disease or developing disease themselves because of their fragile sites.]. 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:11076037;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP412829.RAvkKiRHTebcvYQT9AXS7h5zVnrWq5jDcQ37gWcBEBGVs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:40+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}