@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk> .
@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:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_head {
  this: np:hasAssertion dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_assertion;
    np:hasProvenance dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_provenance;
    np:hasPublicationInfo dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_assertion a np:Assertion .
  
  dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_provenance a np:Provenance .
  
  dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_assertion {
  miriam-gene:1387 a ncit:C16612 .
  
  lld:C0080178 a ncit:C7057 .
  
  dgn-gda:DGN81d1d3d840efcb85bfb04f47ec75b70f sio:SIO_000628 miriam-gene:1387, lld:C0080178;
    a sio:SIO_001122 .
}

dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_provenance {
  dgn-np:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_assertion dcterms:description
      "[Modest associations were observed in CITED2, EP300, CREBBP, TFAP2A and CARM1 but not ALX1. However, these modest associations were not statistically significant after correction for multiple comparisons. Searching for potential functional variants and rare causal mutations is warranted in these 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:20932315;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP89227.RAzGpFDuHTHSbQQVyv2v4myTXjPmGXMfA7FDCTTBZpOAk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:44+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" .
}