@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4> .
@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:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_head {
  this: np:hasAssertion dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_assertion;
    np:hasProvenance dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_provenance;
    np:hasPublicationInfo dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_assertion a np:Assertion .
  
  dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_provenance a np:Provenance .
  
  dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_assertion {
  miriam-gene:6489 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN27ca2f58279fece76c58d930b8e3acc1 sio:SIO_000628 miriam-gene:6489, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_provenance {
  dgn-np:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_assertion dcterms:description
      "[A study of 274 family trios (affected child and both unaffected parents) from Australia validated the association of ST8SIA1 in individuals with MS, showing transmission disequilibrium of the paternal alleles for three additional SNPs, namely rs704219, rs2041906, and rs1558793, with p = 0.001, p = 0.01 and p = 0.01 respectively.]. 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:18612409;
    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:NP81669.RAKZrGnsyclGn7Qbt-mFdCT-3wtJN61gnzEQp2uZmDdS4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:40+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" .
}