@prefix dct: <http://purl.org/dc/terms/> .
@prefix this: <http://purl.org/np/RAQCBxNH_FcdReyKPOnM6FwCkp97dh1Ebq-4d8SAEHd0I> .
@prefix sub: <http://purl.org/np/RAQCBxNH_FcdReyKPOnM6FwCkp97dh1Ebq-4d8SAEHd0I#> .
@prefix has-source: <http://semanticscience.org/resource/SIO_000253> .
@prefix refers-to: <http://semanticscience.org/resource/SIO_000628> .
@prefix gene-disease-association: <http://semanticscience.org/resource/SIO_000983> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix wd: <https://www.wikidata.org/entity/> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pmid: <http://identifiers.org/pubmed/> .
@prefix pav: <http://purl.org/pav/> .
@prefix ensembl: <http://identifiers.org/ensembl/> .
@prefix omim: <http://identifiers.org/omim/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix orcid: <http://orcid.org/> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .

sub:head {
	this: np:hasAssertion sub:assertion ;
		np:hasProvenance sub:provenance ;
		np:hasPublicationInfo sub:publicationInfo ;
		a np:Nanopublication .
}

sub:assertion {
	ensembl:ENSG00000179915 a ncit:C16612 ;
		rdfs:label "NRXN1" .
	
	sub:association refers-to: ensembl:ENSG00000179915 , omim:614325 ;
		a gene-disease-association: .
}

sub:provenance {
	pmid:19896112 dct:title "CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila" .
	
	sub:assertion has-source: pmid:19896112 .
}

sub:publicationInfo {
	sub:activity a prov:Activity ;
		prov:atLocation wd:Q1137652 .
	
	this: dct:created "2018-04-05T10:17:11.353+02:00"^^xsd:dateTime ;
		dct:rights <http://creativecommons.org/publicdomain/zero/1.0/> ;
		pav:authoredBy orcid:0000-0001-6048-1457 , orcid:0000-0002-7770-620X ;
		pav:createdBy orcid:0000-0001-7542-0286 ;
		prov:wasGeneratedBy sub:activity .
}