@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM> .
@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:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_head {
  this: np:hasAssertion dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion;
    np:hasProvenance dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance;
    np:hasPublicationInfo dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion a np:Assertion .
  
  dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance a np:Provenance .
  
  dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_assertion {
  miriam-gene:7461 a ncit:C16612 .
  
  lld:C0175702 a ncit:C7057 .
  
  dgn-gda:DGN950c1b63ee293940cf877211ab10214f sio:SIO_000628 miriam-gene:7461, lld:C0175702;
    a sio:SIO_001121 .
}

dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_provenance {
  dgn-np:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_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-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:NP242874.RAUcr9cDgfRpG26zpHyP9dLgVcChno6tX7e8oj0xDtKlM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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" .
}