@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q> .
@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:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_head {
  this: np:hasAssertion dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion;
    np:hasProvenance dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance;
    np:hasPublicationInfo dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion a np:Assertion .
  
  dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance a np:Provenance .
  
  dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion {
  miriam-gene:1137 a ncit:C16612 .
  
  lld:C0027765 a ncit:C7057 .
  
  dgn-gda:DGN36cf104d046d2afd2f69fbec95548df3 sio:SIO_000628 miriam-gene:1137, lld:C0027765;
    a sio:SIO_001121 .
}

dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance {
  dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion dcterms:description
      "[Understanding of the molecular basis of paroxysmal disorders affecting the central nervous system has been revolutionalized with the identification of mutations in genes for the neurotransmitter receptors, GLRA1 and CHRNA4, and a voltage-gated potassium channel, KCNA1, as causes of inherited neurological disease.]. 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:7620586;
    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:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:05+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" .
}