@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP916096.RA9ACTF06kC_ndXj-WFXbbomVuoiIXPYrxegKiEwUVm-U> .
@prefix sub: <http://rdf.disgenet.org/resource/nanopub/NP916096.RA9ACTF06kC_ndXj-WFXbbomVuoiIXPYrxegKiEwUVm-U#> .
@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 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-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v5.0.0/void/> .

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

sub:assertion {
	dgn-gda:DGN150b81b3a9190edba72d85bae14db345 sio:SIO_000628 miriam-gene:6261 , lld:C0024591 ;
		a sio:SIO_001122 .
}

sub:provenance {
	sub:assertion dcterms:description "[The identification of novel RYR1 variants and previously observed RYR1 variants of uncertain significance in independent MHS families is necessary for demonstrating the significance of these variants for MH susceptibility and supports the need for functional studies of these variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
		wi:evidence dgn-void:source_evidence_curated ;
		sio:SIO_000772 miriam-pubmed:23558838 ;
		prov:wasDerivedFrom dgn-void:UNIPROT ;
		prov:wasGeneratedBy eco:ECO_0000218 .
	
	dgn-void:UNIPROT pav:importedOn "2017-01-25"^^xsd:date .
	
	dgn-void:source_evidence_curated a eco:ECO_0000205 ;
		rdfs:comment "Gene-disease associations manually curated."@en ;
		rdfs:label "DisGeNET evidence - CURATED"@en .
}

sub:publicationInfo {
	this: dcterms:created "2017-10-17T13:16:01+02:00"^^xsd:dateTime ;
		dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
		dcterms:rightsHolder dgn-void:IBIGroup ;
		dcterms:subject sio:SIO_000983 ;
		prv:usedData dgn-void:disgenetv3.0rdf ;
		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> ;
		pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
		pav:version "v5.0.0.0" .
	
	dgn-void:disgenetv3.0rdf pav:version "v5.0.0" .
}