@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU> .
@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:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_head {
   this: np:hasAssertion dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_assertion ;
    np:hasProvenance dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_provenance ;
    np:hasPublicationInfo dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_assertion a np:Assertion .
  dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_provenance a np:Provenance .
  dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_assertion {
   miriam-gene:6329 a ncit:C16612 .
  lld:C0026848 a ncit:C7057 .
  dgn-gda:DGNc1381ad97af4ec6ba4a1c48297a2fb97 sio:SIO_000628 miriam-gene:6329 , lld:C0026848 ;
    a sio:SIO_001122 .
}
dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_provenance {
   dgn-np:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_assertion dcterms:description "[The present study is to observe in vitro the proliferation ability of the muscle cells from permanent myopathy (PM) patients of nomokalaemic periodic paralysis (normKPP), which is caused by mutations of Met1592Val in the skeletal muscle voltage gated sodium channel (SCN4A) gene on chromosome 17q23.1.]. 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:19290024 ;
    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:NP726498.RAaJ3tZsMCEICANG8D1TqhYACb_HIr9N0aE9ehlV7Q1wU130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:14+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}