@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U> .
@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:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_head {
  this: np:hasAssertion dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_assertion ;
    np:hasProvenance dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_provenance ;
    np:hasPublicationInfo dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_assertion a np:Assertion .
  dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_provenance a np:Provenance .
  dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_assertion {
  miriam-gene:93986 a ncit:C16612 .
  lld:C1510586 a ncit:C7057 .
  dgn-gda:DGNb4f59b78b204563eea28903135ce438c sio:SIO_000628 miriam-gene:93986 , lld:C1510586 ;
    a sio:SIO_001121 .
}
dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_provenance {
  dgn-np:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_assertion dcterms:description "[After a brief overview of this field of research and the neural basis of primate vocalizations, we review studies that have addressed the genetic basis of usage and structure of ultrasonic communication in mice, with a focus on the gene FOXP2 involved in specific language impairments and neuroligin genes (NL-3 and NL-4) involved in autism spectrum disorders.]. 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:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP821533.RAXClLIhM1FfIDTXYpCvdgPVZa0_H5Yc1JsqMmd4KyV9U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:57+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}