@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw> .
@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:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_head {
  this: np:hasAssertion dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_assertion;
    np:hasProvenance dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_provenance;
    np:hasPublicationInfo dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_assertion a np:Assertion .
  
  dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_provenance a np:Provenance .
  
  dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_assertion {
  miriam-gene:8301 a ncit:C16612 .
  
  lld:C0494463 a ncit:C7057 .
  
  dgn-gda:DGN1705740c6965fc24fb6197bc8c6999d3 sio:SIO_000628 miriam-gene:8301, lld:C0494463;
    a sio:SIO_001121 .
}

dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_provenance {
  dgn-np:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_assertion dcterms:description
      "[In order to evaluate association with these genome-wide association study-identified genes and to isolate the variants contributing to the pathogenesis of LOAD, we genotyped the top single nucleotide polymorphisms (SNPs), rs11136000 (CLU), rs3818361 (CR1), and rs3851179 (PICALM), and sequenced the entire coding regions of these genes in our cohort of 342 LOAD patients and 277 control subjects.]. 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:22402018;
    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:NP387900.RAWJ4i1srenydc2yQfs1yDv6xRpB0d-2q4MRs8OW8kUqw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}