@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8> .
@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:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_head {
  this: np:hasAssertion dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion;
    np:hasProvenance dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance;
    np:hasPublicationInfo dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion a np:Assertion .
  
  dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance a np:Provenance .
  
  dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion {
  miriam-gene:5663 a ncit:C16612 .
  
  lld:C0233794 a ncit:C7057 .
  
  dgn-gda:DGN28e8ee03acf6f83f9df1215889b34a00 sio:SIO_000628 miriam-gene:5663, lld:C0233794;
    a sio:SIO_001121 .
}

dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_provenance {
  dgn-np:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_assertion dcterms:description
      "[These results suggest that the sensorimotor gating is impaired with the progressing of AD phenotype, and its deficit may be correlated to cerebral Aβ neuropathology and memory impairment in the APP/PS1 transgenic mouse model of AD.]. 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:22595040;
    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:NP467870.RAv3aYvo7SFvMS3454464RW73WQNBy1Y0Nm4de3ABv7A8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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" .
}