@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o> .
@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:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_head {
  this: np:hasAssertion dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_assertion ;
    np:hasProvenance dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_provenance ;
    np:hasPublicationInfo dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_assertion a np:Assertion .
  dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_provenance a np:Provenance .
  dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_assertion {
  miriam-gene:2332 a ncit:C16612 .
  lld:C0233794 a ncit:C7057 .
  dgn-gda:DGN8ceafad55a89c4b3643bc19c91f37923 sio:SIO_000628 miriam-gene:2332 , lld:C0233794 ;
    a sio:SIO_001121 .
}
dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_provenance {
  dgn-np:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_assertion dcterms:description "[Using high-resolution behavioral, genetic, and biochemical analyses, we present evidence that excess mGluR upon FMRP attenuation is linked to the cAMP decrement reported in patients and models, and underlies olfactory associative learning and memory deficits.]. 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:22993428 ;
    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:NP622001.RApVSb3tMaWZoxcH9-OGpTuQxRCPTdZHg4obJhl_KWn2o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:15+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> ;
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}