@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0> .
@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:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_head {
  this: np:hasAssertion dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_assertion ;
    np:hasProvenance dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_provenance ;
    np:hasPublicationInfo dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_assertion a np:Assertion .
  dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_provenance a np:Provenance .
  dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_assertion {
  miriam-gene:6329 a ncit:C16612 .
  lld:C0004093 a ncit:C7057 .
  dgn-gda:DGNbd6a3e03a75beecf93056c09887a19ea sio:SIO_000628 miriam-gene:6329 , lld:C0004093 ;
    a sio:SIO_001121 .
}
dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_provenance {
  dgn-np:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_assertion dcterms:description "[In a large family with historic data on seven generations and a clear phenotype, including myotonia at movement onset, with worsening by cold temperature, pregnancy, mental stress, and especially after rest after intense physical activity, but without weakness, the phenotype was linked with the muscle sodium channel gene (SCN4A) locus, in which a novel p.I141V mutation was found.]. 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:19015483 ;
    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:NP884155.RA-3v4DfoHv1niBZl1boMRMmeDEjmXAP7zCVIgbBhkbN0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:00+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" .
}