@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4> .
@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:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_head {
  this: np:hasAssertion dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_assertion ;
    np:hasProvenance dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_provenance ;
    np:hasPublicationInfo dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_provenance a np:Provenance .
  dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_assertion {
  miriam-gene:51172 a ncit:C16612 .
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}
dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_provenance {
  dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_assertion dcterms:description "[This, together with the different brain expression patterns of GNPTAB, GNPTG, and NAGPA compared to that of FOXP2 and CNTNAP2, suggests that the genetic neuropathological origins of stuttering differ from those of verbal dyspraxia and SLI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
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}
dgn-np:NP1180431.RAOpPVtq1iKG7t15IA98qENg3DMBN4OkQ6wKOE-mUphh4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:41+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    pav:version "v4.0.0.0" .
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}