@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas> .
@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:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_head {
  this: np:hasAssertion dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_assertion;
    np:hasProvenance dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_provenance;
    np:hasPublicationInfo dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_assertion a np:Assertion .
  
  dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_provenance a np:Provenance .
  
  dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0162635 a ncit:C7057 .
  
  dgn-gda:DGNf3a27551ce17270c838a4df534f0f7bb sio:SIO_000628 miriam-gene:3342, lld:C0162635;
    a sio:SIO_001121 .
}

dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_provenance {
  dgn-np:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_assertion dcterms:description
      "[These patients illustrate the expanding spectrum of molecular findings in AS, reinforce the need to maintain suspicion when clinical features suggest AS but initial testing is normal, and show the power of CGH as a tool to uncover partial UBE3A deletions.]. 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:17036311;
    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:NP573268.RAwq3XqLDZsV7fmdRZjtHEAi3w-BehCDveeEd4kwdRLas130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}