@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk> .
@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/v4.0.0/void/> .

dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_head {
  this: np:hasAssertion dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion;
    np:hasProvenance dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance;
    np:hasPublicationInfo dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion a np:Assertion .
  
  dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance a np:Provenance .
  
  dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion {
  miriam-gene:3274 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN2335da9579e79ec77efd313d5fb3de5a sio:SIO_000628 miriam-gene:3274, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_provenance {
  dgn-np:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_assertion dcterms:description
      "[We have concluded that the participation of these variants in the disorder is unlikely, particularly in view of their apparent lack of function and unlikely influence on receptor expression. However their nature alludes to the potential presence of other ]. 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:12429384;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP77043.RA6l7DNRO0-XLtzyCY5Bq-78LHCaqhrM9Av9XZDkLHZFk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:23+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}