@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE> .
@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:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_head {
  this: np:hasAssertion dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_assertion;
    np:hasProvenance dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_provenance;
    np:hasPublicationInfo dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_assertion a np:Assertion .
  
  dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_provenance a np:Provenance .
  
  dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_assertion {
  miriam-gene:4204 a ncit:C16612 .
  
  lld:C0035372 a ncit:C7057 .
  
  dgn-gda:DGN186c614100990ea828cab77fedd36508 sio:SIO_000628 miriam-gene:4204, lld:C0035372;
    a sio:SIO_001121 .
}

dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_provenance {
  dgn-np:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_assertion dcterms:description
      "[Our high mutation detection rate, compared to two of the previous studies, underscores the importance of the inclusion criteria of the patients and supports that MECP2 is the most important, if not the only, gene responsible for RTT.]. 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:11313756;
    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:NP177368.RAGGen3ghYoTwGxBQ9Dlco6ULLlcUnyaCSx53yUvcUAtE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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" .
}