@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM> .
@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:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_head {
  this: np:hasAssertion dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_assertion;
    np:hasProvenance dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_provenance;
    np:hasPublicationInfo dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_assertion a np:Assertion .
  
  dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_provenance a np:Provenance .
  
  dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGNf18103a87e5c7f0ae7046c6782adc728 sio:SIO_000628 miriam-gene:4397, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_provenance {
  dgn-np:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_assertion dcterms:description
      "[It can be occur in neurodegenerative disorders, such as Parkinson's disease, Huntington's and Alzheimer's disease, in stroke, in epilepsy, in multiple sclerosis, in amyotrophic lateral sclerosis, and in mental failures, such as schizophrenia and depression.]. 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:17017544;
    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:NP728963.RAfl1NiHHDJJynW4YO8sLWzw71Db69PManSiewYl3YQFM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:22+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" .
}