@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo> .
@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:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_head {
  this: np:hasAssertion dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion ;
    np:hasProvenance dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance ;
    np:hasPublicationInfo dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion a np:Assertion .
  dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance a np:Provenance .
  dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion {
  miriam-gene:4204 a ncit:C16612 .
  lld:C0035372 a ncit:C7057 .
  dgn-gda:DGN76a1b2e2d77cc609ec2be0da887135ec sio:SIO_000628 miriam-gene:4204 , lld:C0035372 ;
    a sio:SIO_001121 .
}
dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_provenance {
  dgn-np:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_assertion dcterms:description "[Reversal of phenotypes in adult symptomatic mice has been demonstrated in some models of monogenic loss-of-function neurological disorders, including loss of MeCP2 in Rett syndrome, indicating that, at least in some cases, the neuroanatomy may remain sufficiently intact so that correction of the molecular dysfunction underlying these disorders can restore healthy physiology.]. 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:26605526 ;
    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:NP1295630.RABUns_8YeEBlz9bLjfSpOIkpKIQozgNrHVu7DMtPGpeo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:33+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" .
}