@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_head {
  this: np:hasAssertion dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_assertion;
    np:hasProvenance dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_provenance;
    np:hasPublicationInfo dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_assertion a np:Assertion .
  
  dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_provenance a np:Provenance .
  
  dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_assertion {
  miriam-gene:923 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGNfdbfd016251fb1a979dc7d3889b5569a sio:SIO_000628 miriam-gene:923, lld:C0026769;
    a sio:SIO_001122 .
}

dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_provenance {
  dgn-np:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_assertion dcterms: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 othe]. 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-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP189327.RAcVTLud5SCJARSLF2d9LgBDWJZQcgZ5qOgqJAT4jKbEk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:13+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}