@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg> .
@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:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_head {
  this: np:hasAssertion dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion;
    np:hasProvenance dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance;
    np:hasPublicationInfo dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion a np:Assertion .
  
  dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance a np:Provenance .
  
  dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion {
  miriam-gene:161582 a ncit:C16612 .
  
  lld:C0476254 a ncit:C7057 .
  
  dgn-gda:DGNf2d995f661a23668d4eb88c93662cd09 sio:SIO_000628 miriam-gene:161582, lld:C0476254;
    a sio:SIO_001121 .
}

dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_provenance {
  dgn-np:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_assertion dcterms:description
      "[Within two of these loci, DYX1C1 (15q21) and ROBO1 (3p12) have recently been proposed as dyslexia candidate genes through the molecular analysis of translocation breakpoints in dyslexic individuals carrying balanced chromosomal translocations.]. 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:18521840;
    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:NP977259.RABv50SnSRNdoHRqAni_hql-Rt15--Pq86Vvl9qxkMiNg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:37+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" .
}