@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I> .
@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:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_head {
  this: np:hasAssertion dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_assertion;
    np:hasProvenance dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_provenance;
    np:hasPublicationInfo dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_assertion a np:Assertion .
  
  dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_provenance a np:Provenance .
  
  dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_assertion {
  miriam-gene:79813 a ncit:C16612 .
  
  lld:C1510586 a ncit:C7057 .
  
  dgn-gda:DGN1c159eb1cb54473af5c49389d17168d9 sio:SIO_000628 miriam-gene:79813, lld:C1510586;
    a sio:SIO_001121 .
}

dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_provenance {
  dgn-np:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_assertion dcterms:description
      "[Comparisons between the observed shared clinical features and molecular analyses in 20 subjects suggest that increased dosage of EHMT1 may be responsible for the neurodevelopmental impairment, speech delay, and autism spectrum disorders revealing the dosage sensitivity of yet another chromatin remodeling protein in human disease.]. 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:22890305;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1004900.RAPddfdgE6eG19_eD-YBTYvE1kzk_LOuPcFNbeT-B0j9I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:21+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" .
}