@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_head { this: np:hasAssertion dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_assertion; np:hasProvenance dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_provenance; np:hasPublicationInfo dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_publicationInfo; a np:Nanopublication . dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_assertion a np:Assertion . dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_provenance a np:Provenance . dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_assertion { miriam-gene:26047 a ncit:C16612 . lld:C0038506 a ncit:C7057 . dgn-gda:DGN7a97f183fb336406979fc81b815a089a sio:SIO_000628 miriam-gene:26047, lld:C0038506; a sio:SIO_001121 . } dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_provenance { dgn-np:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_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; sio:SIO_000772 miriam-pubmed:24807205; prov:wasDerivedFrom dgn-void:befree-2016; 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:NP1180437.RAomJyztR8QMWT-VTX6OCfDRU82_00h_vOcYChPexlJCw130_publicationInfo { this: dcterms:created "2016-05-13T12:50:41+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }