@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E> .
@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:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_head {
  this: np:hasAssertion dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_assertion;
    np:hasProvenance dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_provenance;
    np:hasPublicationInfo dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_assertion a np:Assertion .
  
  dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_provenance a np:Provenance .
  
  dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_assertion {
  miriam-gene:1797 a ncit:C16612 .
  
  lld:C0795864 a ncit:C7057 .
  
  dgn-gda:DGNf4d954cd17b2360dd89b9f7e01a33eab sio:SIO_000628 miriam-gene:1797, lld:C0795864;
    a sio:SIO_001121 .
}

dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_provenance {
  dgn-np:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_assertion dcterms:description
      "[However, we cannot rule out the possibility that cis effects between multiple haploinsufficient genes in the SMS critical interval (e.g., RAI1 and DEXRAS1) either exacerbate the circadian phenotypes observed in SMS patients with deletions or increase their penetrance in certain environments.]. 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:23703963;
    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:NP546215.RAnMdy-NZW-6lIpsPBapS-XbUTaMjNPILRceG3Wvsu69E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:29+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" .
}