@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_head {
  this: np:hasAssertion dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_assertion;
    np:hasProvenance dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_provenance;
    np:hasPublicationInfo dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_assertion a np:Assertion .
  
  dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_provenance a np:Provenance .
  
  dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_assertion {
  miriam-gene:26353 a ncit:C16612 .
  
  lld:C0007959 a ncit:C7057 .
  
  dgn-gda:DGN16c7d869fc073537c100b6865c8f140c sio:SIO_000628 miriam-gene:26353, lld:C0007959;
    a sio:SIO_001121 .
}

dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_provenance {
  dgn-np:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_assertion dcterms:description
      "[A number of missense mutations in the two related small heat shock proteins HspB8 (Hsp22) and HspB1 (Hsp27) have been associated with the inherited motor neuron diseases (MND) distal hereditary motor neuropathy and Charcot-Marie-Tooth 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:20157854;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP883122.RAzMuovzDH2ZeLo0-jKtFFKF0WWuEUbNOuumLTY4_cpDc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:38+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}