@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A> .
@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:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_head {
  this: np:hasAssertion dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_assertion;
    np:hasProvenance dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_provenance;
    np:hasPublicationInfo dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_assertion a np:Assertion .
  
  dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_provenance a np:Provenance .
  
  dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_assertion {
  miriam-gene:477 a ncit:C16612 .
  
  lld:C0154723 a ncit:C7057 .
  
  dgn-gda:DGN96d1d04a64e4e49e450eeab51fadd7f7 sio:SIO_000628 miriam-gene:477, lld:C0154723;
    a sio:SIO_001121 .
}

dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_provenance {
  dgn-np:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_assertion dcterms:description
      "[The shared hemiplegic migraine phenotype of mutations in ATP1A2 and CACNA1A raises the possibility that they coordinately regulate ion homeostasis that determines susceptibility to the initiation of both migraine aura and the pain phase of migraine.]. 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:14624354;
    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:NP246506.RAwijxkYygv5Vo7tgtAEB2lyIouePM5FkXeKmB1dB7g7A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}