@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0> .
@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:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_head {
  this: np:hasAssertion dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion;
    np:hasProvenance dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance;
    np:hasPublicationInfo dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion a np:Assertion .
  
  dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance a np:Provenance .
  
  dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion {
  miriam-gene:4763 a ncit:C16612 .
  
  lld:C0027765 a ncit:C7057 .
  
  dgn-gda:DGNa78aa4d5a03826120cb47871897e3ad4 sio:SIO_000628 miriam-gene:4763, lld:C0027765;
    a sio:SIO_001121 .
}

dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_provenance {
  dgn-np:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_assertion dcterms:description
      "[The molecular defects responsible for Huntington's disease, the spinocerebellar degenerations, myotonic muscular dystrophy, neurofibromatosis, and tuberous sclerosis, among other major dominant inherited diseases of the nervous system, will be identified using the new techniques of molecular genetics.]. 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:6378063;
    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:NP684234.RAgtLFsWaY55s4rXWk6vJ35j88WPSPtk-2bR9vKB-pav0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:56+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" .
}