@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0> .
@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 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:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_head {
  this: np:hasAssertion dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion;
    np:hasProvenance dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance;
    np:hasPublicationInfo dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion a np:Assertion .
  
  dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance a np:Provenance .
  
  dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion {
  miriam-gene:596 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN696e8a499c346fc42e3f57e136aa661a sio:SIO_000628 miriam-gene:596, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_provenance {
  dgn-np:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_assertion dct:description
      "[No significant differences in the frequency of gene sequence variations were found between MS patients and controls. The apoptosis genes studied here therefore appear less likely to be important effector genes in MS.]. 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:12161031;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47856.RAq26o8YWoh9cGYfMteBU6QHSIbkjDB7OijTRgEhSNqW0130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}