@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_head {
  this: np:hasAssertion dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_assertion;
    np:hasProvenance dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_provenance;
    np:hasPublicationInfo dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_assertion a np:Assertion .
  
  dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_provenance a np:Provenance .
  
  dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_assertion {
  miriam-gene:6329 a ncit:C16612 .
  
  lld:C1279412 a ncit:C7057 .
  
  dgn-gda:DGN37f3e0e22901a7dc204528a758339b31 sio:SIO_000628 miriam-gene:6329, lld:C1279412;
    a sio:SIO_001121 .
}

dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_provenance {
  dgn-np:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_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-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP682946.RAU4Lc6IQx0t6hLIf3VpNdk5wKsTUlo3dFQIhE9_rzHDQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}