@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y> .
@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:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_head {
  this: np:hasAssertion dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_assertion ;
    np:hasProvenance dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_assertion a np:Assertion .
  dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_provenance a np:Provenance .
  dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_assertion {
  miriam-gene:3786 a ncit:C16612 .
  lld:C0085541 a ncit:C7057 .
  dgn-gda:DGNc573dbfb5e312c07812e8d630a502ee0 sio:SIO_000628 miriam-gene:3786 , lld:C0085541 ;
    a sio:SIO_001121 .
}
dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_provenance {
  dgn-np:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_assertion dcterms:description "[Disease gene identification, such as the two potassium ion channels (KCNQ2 and KCNQ3) for the two forms of benign familial neonatal seizures (BFNC) and the alpha4 subunit of the nicotinic receptor for autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), however, should yield significant advances in drug discoveries.]. 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:10716662 ;
    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:NP489073.RAleWt0O_pAMxWKqeDmDOp44Ylw7pyjoPV3KpZWjxOG_Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+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" .
}