@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg> .
@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:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_head {
  this: np:hasAssertion dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_assertion;
    np:hasProvenance dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_provenance;
    np:hasPublicationInfo dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_assertion a np:Assertion .
  
  dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_provenance a np:Provenance .
  
  dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_assertion {
  miriam-gene:23327 a ncit:C16612 .
  
  lld:C0476254 a ncit:C7057 .
  
  dgn-gda:DGN8c25d50317d4aaeb53a0443f51c58bde sio:SIO_000628 miriam-gene:23327, lld:C0476254;
    a sio:SIO_001121 .
}

dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_provenance {
  dgn-np:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_assertion dcterms:description
      "[In summary, our results substantiate genetic markers in NEDD4L and MYO5B as risk factors for dyslexia and provide first evidence that the relevance of these markers is not restricted to the English language.]. 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:24373531;
    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:NP870901.RAOE3i8wUN358OhNRm1BZUX_n_EmqN086SgCV40Ch_mpg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:29+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" .
}