@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY> .
@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:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_head {
  this: np:hasAssertion dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_assertion;
    np:hasProvenance dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_provenance;
    np:hasPublicationInfo dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_assertion a np:Assertion .
  
  dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_provenance a np:Provenance .
  
  dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_assertion {
  miriam-gene:965 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNb6bfe215268472927a1bda494ff72a2d sio:SIO_000628 miriam-gene:965, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_provenance {
  dgn-np:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_assertion dc:description
      "[The primary interest in the MSGB concept resides in its capacity to integrate cumulative genetic contributions to MS risk. This analysis underlines the high variability of family load with known common variants. This novel approach can be extended to other genetically complex diseases. Despite the emphasis on assembling large case-control datasets, multigenerational, multiaffected families remain an invaluable resource for advancing the understanding of the genetic architecture of complex traits.]. 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:21280076;
    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:NP78600.RASmvwyQdDB_4Z2RygSxvbcAMoQaohjq7kvdHMd8fQMyY130_publicationInfo {
  this: dc:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}