@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_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:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_head {
   this: np:hasAssertion dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_assertion ;
    np:hasProvenance dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_provenance ;
    np:hasPublicationInfo dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_assertion a np:Assertion .
  dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_provenance a np:Provenance .
  dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_assertion {
   miriam-gene:200959 a ncit:C16612 .
  lld:C3543433 a ncit:C7057 .
  dgn-gda:DGN873fad0cab3758556a971238a0e09180 sio:SIO_000628 miriam-gene:200959 , lld:C3543433 ;
    a sio:SIO_001122 .
}
dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_provenance {
   dgn-np:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_assertion dcterms:description "[To investigate the possible association between the GABA receptor subtype rho1, rho2, and rho3 (GABRR1, GABRR2, and GABRR3) genotypes and allelic variants of the single nucleotide polymorphisms GABRR1-M26V (Met26Val, rs12200969), GABRR1-H27R (His26Arg, rs1186902), GABRR2-T455M (Thr55Met, rs282129), and GABRR3-Y205X (Tyr205X, rs832032), and the risk for ET, we studied the frequency of the previously mentioned GABRR genotypes and allelic variants in 200 patients with ET and 250 healthy controls using TaqMan genotyping.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20150227 ;
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  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:NP979381.RAyNg8hmXKTFX1wwu4Qeg2TDOPd6T1VMwN0hZ6CHxPx_c130_publicationInfo {
   this: dcterms:created "2015-08-25T14:47:38+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    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> ;
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}