@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg> .
@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:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_head {
  this: np:hasAssertion dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion;
    np:hasProvenance dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance;
    np:hasPublicationInfo dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion a np:Assertion .
  
  dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance a np:Provenance .
  
  dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C0338656 a ncit:C7057 .
  
  dgn-gda:DGNf7699e76fa947931887d78c6cc8b2b19 sio:SIO_000628 miriam-gene:1437, lld:C0338656;
    a sio:SIO_001121 .
}

dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance {
  dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion dcterms:description
      "[The observation that genetic risk variants are associated with thickness across AD-vulnerable regions of interest in CN older individuals, suggests that the combination of polygenic risk profile, neuroimaging, and CSF biomarkers may hold synergistic potential to aid in the prediction of future cognitive decline.]. 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:22169231;
    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:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:00+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" .
}