@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c> .
@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/v3.0.0/void/> .

dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_head {
  this: np:hasAssertion dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_assertion;
    np:hasProvenance dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_provenance;
    np:hasPublicationInfo dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_assertion a np:Assertion .
  
  dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_provenance a np:Provenance .
  
  dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_assertion {
  miriam-gene:6329 a ncit:C16612 .
  
  lld:C1279412 a ncit:C7057 .
  
  dgn-gda:DGNbada54c9e8c0563fb17b2eb35ff5d095 sio:SIO_000628 miriam-gene:6329, lld:C1279412;
    a sio:SIO_001122 .
}

dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_provenance {
  dgn-np:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_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-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP682878.RAABHp-afPcbm4ERGrqvfQjy8jzc7Pa10KXaSBPlpzX_c130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:31+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}