@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE> .
@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:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_head {
  this: np:hasAssertion dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_assertion;
    np:hasProvenance dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_provenance;
    np:hasPublicationInfo dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_assertion a np:Assertion .
  
  dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_provenance a np:Provenance .
  
  dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_assertion {
  miriam-gene:1967 a ncit:C16612 .
  
  lld:C1858991 a ncit:C7057 .
  
  dgn-gda:DGN343e85afa68907700f69fec9814d1b5e sio:SIO_000628 miriam-gene:1967, lld:C1858991;
    a sio:SIO_001121 .
}

dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_provenance {
  dgn-np:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_assertion dcterms:description
      "[We hypothesized that polymorphisms in EIF2B1-5, the genes involved in VWM, might be risk factors for the development of MS or temperature sensitivity in patients with MS. We found no difference in the frequencies of 15 EIF2B1-5 variants between patients with MS and healthy controls, and none of the variants showed significant deviation of the Hardy-Weinberg equilibrium.]. 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:18632786;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP860578.RA9tXS5Lg_90iI0jiJWBqfQt8dQ-mAmxpMFz_utpMvAAE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:46+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" .
}