@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY> .
@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:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_head {
  this: np:hasAssertion dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_assertion;
    np:hasProvenance dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_provenance;
    np:hasPublicationInfo dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_assertion a np:Assertion .
  
  dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_provenance a np:Provenance .
  
  dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_assertion {
  miriam-gene:4747 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGNa276c9767987cc1e8de25c3f40619d19 sio:SIO_000628 miriam-gene:4747, lld:C0002736;
    a sio:SIO_001122 .
}

dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_provenance {
  dgn-np:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_assertion dcterms:description
      "[mutations in neurofilaments are possible risk factors that may contribute to pathogenesis in amyotrophic lateral sclerosis in conjunction with one or more additional genetic or environmental factors, but are not significant primary causes ]. 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:16084104;
    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:NP140594.RA-J04H_VcvvBG5zBlcP9_0c_3otbRYBjkr9d5jZkXDKY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:13+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" .
}