@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE> .
@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:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_head {
  this: np:hasAssertion dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion;
    np:hasProvenance dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance;
    np:hasPublicationInfo dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion a np:Assertion .
  
  dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance a np:Provenance .
  
  dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion {
  miriam-gene:43 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN99b3e04f4948340404b47924057fcbb6 sio:SIO_000628 miriam-gene:43, lld:C0524851;
    a sio:SIO_001122 .
}

dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance {
  dgn-np:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion dcterms:description
      "[Variant-specific causal involvement of AChE in the progression of both neurodegenerative diseases and neuromuscular syndromes raises the possibility that future therapeutic drugs might target specific AChE variant (s) or the corresponding RNA transcripts.]. 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:16516310;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:11+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" .
}