@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs> .
@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:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_head {
  this: np:hasAssertion dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_assertion;
    np:hasProvenance dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_provenance;
    np:hasPublicationInfo dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_assertion a np:Assertion .
  
  dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_provenance a np:Provenance .
  
  dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_assertion {
  miriam-gene:5310 a ncit:C16612 .
  
  lld:C0041341 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_provenance {
  dgn-np:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_assertion dcterms:description
      "[We have sequenced 1949 kb from the terminal Giemsa light band of human chromosome 16p, enabling us to fully annotate the region extending from the telomeric repeats to the previously published tuberous sclerosis disease 2 (TSC2) and polycystic kidney disease 1 (PKD1) genes.]. 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:11157797;
    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:NP638009.RAQJISw86ZZFGXhrxzAMemjFvj-jw_JFIVuVzbbfc4zzs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:25+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" .
}