@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:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_head { this: np:hasAssertion dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_assertion; np:hasProvenance dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_provenance; np:hasPublicationInfo dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_publicationInfo; a np:Nanopublication . dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_assertion a np:Assertion . dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_provenance a np:Provenance . dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_assertion { miriam-gene:23229 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN6864701109d89af3e64a32745c94bbf1 sio:SIO_000628 miriam-gene:23229, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_provenance { dgn-np:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_assertion dcterms:description "[Gephyrin has well-established functional links with several synaptic proteins that have been implicated in genetic risk for neurodevelopmental disorders such as autism spectrum disorder (ASD), schizophrenia and epilepsy including the neuroligins (NLGN2, NLGN4), the neurexins (NRXN1, NRXN2, NRXN3) and collybistin (ARHGEF9).]. 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:23393157; 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:NP1051384.RAr7NYV4z2XX-JOsxfckC3eZjmQYEO10KmT1oP54MvWYk130_publicationInfo { this: dcterms:created "2016-05-13T12:49:42+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" . }