@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU> .
@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:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_head {
  this: np:hasAssertion dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_assertion ;
    np:hasProvenance dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_provenance ;
    np:hasPublicationInfo dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_provenance a np:Provenance .
  dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_assertion {
  miriam-gene:286676 a ncit:C16612 .
  lld:C0026769 a ncit:C7057 .
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    a sio:SIO_001122 .
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dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_provenance {
  dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_assertion dcterms:description "[We have performed a meta-analysis of GWAS in MS that more than doubles the size of previous gene discovery efforts and highlights 3 novel MS susceptibility loci. These and additional loci with suggestive evidence of association are excellent candidates for further investigations to refine and validate their role in the genetic architecture of MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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dgn-np:NP96700.RAH3AMegt1woLSRQoz1DpIHcgYT_p7oop_E_NngNsE8KU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:49+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 ;
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}