@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc> .
@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 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:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_head {
  this: np:hasAssertion dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion;
    np:hasProvenance dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance;
    np:hasPublicationInfo dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion a np:Assertion .
  
  dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance a np:Provenance .
  
  dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGNe6dbec2af00629d6fcb0401ed6763b8a sio:SIO_000628 miriam-gene:348, lld:C0002736;
    a sio:SIO_001122 .
}

dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_provenance {
  dgn-np:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_assertion dct:description
      "[It was shown that the frequency of the apoE-e2 allele was significantly higher in the young group characterized by more benign course of ALS (spinal variant, slow rate of progression of ALS and longer survival) as well as in patients with a more `benign` spinal form of the 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:19365373;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP71658.RAQH8T1TGiUYpYKve8516qAen7GyS76H6zC6F5xcKaXxc130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}