@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8> .
@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:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_head {
  this: np:hasAssertion dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_assertion;
    np:hasProvenance dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_provenance;
    np:hasPublicationInfo dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_assertion a np:Assertion .
  
  dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_provenance a np:Provenance .
  
  dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_assertion {
  miriam-gene:3984 a ncit:C16612 .
  
  lld:C0175702 a ncit:C7057 .
  
  dgn-gda:DGN707263c312b1b125e38bf4b62bbdc4c5 sio:SIO_000628 miriam-gene:3984, lld:C0175702;
    a sio:SIO_001121 .
}

dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_provenance {
  dgn-np:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_assertion dcterms:description
      "[These data demonstrate abnormalities in HF in WS in agreement with murine models, implicate LIMK1 and CYLN2 in human hippocampal function, and suggest that hippocampal dysfunction may contribute to neurocognitive abnormalities in WS.]. 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:15951840;
    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:NP499099.RAFAnQfecO6HKxQy4CVGT0aSZXqve8SOM3phIBKcjta_8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:31+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" .
}