@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo> .
@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:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_head {
  this: np:hasAssertion dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_assertion ;
    np:hasProvenance dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_provenance ;
    np:hasPublicationInfo dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_publicationInfo ;
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  dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_assertion {
  miriam-gene:9353 a ncit:C16612 .
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dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_provenance {
  dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_assertion dcterms:description "[Based on this, we also propose three novel dyslexia candidate genes (SLIT2, HMGB1 and VAPA) from known linkage regions, and we discuss the possible involvement of genes emerging from the two reported genome-wide association studies for reading impairment-related phenotypes in the identified network.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP846623.RAfjtDryuRtF6kkCl-iycLaObHmKlmv4uEpniAPFsTJCo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:08+02:00"^^xsd:dateTime ;
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