@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc> .
@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:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_head {
  this: np:hasAssertion dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_assertion;
    np:hasProvenance dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_provenance;
    np:hasPublicationInfo dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_assertion a np:Assertion .
  
  dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_provenance a np:Provenance .
  
  dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_assertion {
  miriam-gene:9567 a ncit:C16612 .
  
  lld:C0016667 a ncit:C7057 .
  
  dgn-gda:DGNb150fe51130f285d625293fde05e9ebf sio:SIO_000628 miriam-gene:9567, lld:C0016667;
    a sio:SIO_001121 .
}

dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_provenance {
  dgn-np:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_assertion dcterms:description
      "[This excess can be corrected by reducing signaling by Gp1 mGluRs, and numerous studies have shown that inhibition of mGluR5, in particular, can ameliorate multiple mutant phenotypes in animal models of FXS.]. 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:21090964;
    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:NP703962.RArOGJ5Spqknd_isesRclNXgYHr7wm1Bc1TtXDO7EM0nc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}