@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE> .
@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:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_head {
  this: np:hasAssertion dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_assertion;
    np:hasProvenance dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_provenance;
    np:hasPublicationInfo dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_assertion a np:Assertion .
  
  dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_provenance a np:Provenance .
  
  dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_assertion {
  miriam-gene:55640 a ncit:C16612 .
  
  lld:C0151313 a ncit:C7057 .
  
  dgn-gda:DGNb51614d9a89cc275ee0c4297c78d2736 sio:SIO_000628 miriam-gene:55640, lld:C0151313;
    a sio:SIO_001121 .
}

dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_provenance {
  dgn-np:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_assertion dcterms:description
      "[In this candidate interval, the Cct5 gene encoding the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (CCT) was the most obvious candidate gene since mutation in the Cct4 gene encoding the CCT delta subunit has been reported to be associated with autosomal recessive mutilating sensory neuropathy in mutilated foot (mf) rat mutant.]. 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:16399879;
    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:NP935742.RAA_E53WW_y61YZPkTgxwmKzppwObkKxIrvRR47aOMcHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:33+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" .
}