@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk> .
@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:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_head {
  this: np:hasAssertion dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion;
    np:hasProvenance dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance;
    np:hasPublicationInfo dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion a np:Assertion .
  
  dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance a np:Provenance .
  
  dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion {
  miriam-gene:4803 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN13cddc79050faa8b873b374d9d2bf7f3 sio:SIO_000628 miriam-gene:4803, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_provenance {
  dgn-np:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_assertion dcterms:description
      "[Most Tg AD models, which at least partly recapitulate the AD phenotype, are based on insertion of one or more human mutations (identified in Familial AD) into the mouse genome, with the notable exception of the anti-NGF mouse, which is based on the cholinergic unbalance hypothesis.]. 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:21732714;
    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:NP907433.RAMJ1tj-JwEwB7L5MhBHFgnwk9EileydkMejDc08ThxRk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:35+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" .
}