@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4> .
@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:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_head {
  this: np:hasAssertion dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_assertion;
    np:hasProvenance dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_provenance;
    np:hasPublicationInfo dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_assertion a np:Assertion .
  
  dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_provenance a np:Provenance .
  
  dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN5072f243c91c5e7e10c7b46a6e143ccc sio:SIO_000628 miriam-gene:2332, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_provenance {
  dgn-np:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_assertion dcterms:description
      "[Broad screening for premutation alleles in Parkinson disease populations is unlikely to be productive in the absence of additional clinical or family history data that suggest involvement of the FMR1 gene.]. 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:17620491;
    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:NP726136.RAUFmnvp2C2uA1KHESS4JaID9pFQDvCLWtmfpw7hSXHP4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:20+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" .
}