@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE> .
@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:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_head {
  this: np:hasAssertion dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion;
    np:hasProvenance dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance;
    np:hasPublicationInfo dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion a np:Assertion .
  
  dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance a np:Provenance .
  
  dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion {
  miriam-gene:2006 a ncit:C16612 .
  
  lld:C0243050 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_provenance {
  dgn-np:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_assertion dcterms:description
      "[Molecular genetic studies have shown that deletion at the elastin gene may account for the cardiovascular abnormalities seen in WS, but autistic features are likely caused by other genes flanking elastin.]. 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:16861145;
    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:NP496839.RATyhCrBPxCBrGjqvm9VBBkzHd8TfqrfXgdQbJ6ZcUNwE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:56+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" .
}