@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok> .
@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:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_head {
  this: np:hasAssertion dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_assertion ;
    np:hasProvenance dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_provenance ;
    np:hasPublicationInfo dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_assertion a np:Assertion .
  dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_provenance a np:Provenance .
  dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_assertion {
  miriam-gene:1555 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_provenance {
  dgn-np:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_assertion dcterms:description "[Using PCR and restriction digest analysis, the frequencies of the variant cytochrome P450 debrisoquine hydroxylase CYP2D6 alleles CYP2D6(A) and CYP2D6(B) were investigated in 50 patients with amyotrophic lateral sclerosis (ALS) and 13 patients with ALS and frontotemporal dementia (FTD) and compared to those frequencies in patients with FTD alone and Alzheimer's disease (AD).]. 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:8731176 ;
    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:NP364429.RAvN246R92HbLjn02tEEVV9YKUep518sxOWMy-gXSeBok130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:33+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 ;
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    pav:version "v2.1.0.0" .
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}