@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8> .
@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:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_head {
  this: np:hasAssertion dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_assertion;
    np:hasProvenance dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_provenance;
    np:hasPublicationInfo dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_assertion a np:Assertion .
  
  dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_provenance a np:Provenance .
  
  dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_assertion {
  miriam-gene:3976 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN024988311aed6206e9495c233c61bd0f sio:SIO_000628 miriam-gene:3976, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_provenance {
  dgn-np:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_assertion dcterms:description
      "[The results indicate that the LIF 3' UTR StuI polymorphism is not associated with multiple sclerosis, however we cannot exclude the hypothesis that other polymorphic alleles of LIF could be implicated in MS susceptibility.]. 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:19251277;
    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:NP454191.RAaVylUCBzoFZGClhQN3qnpGX1yPZfy5SpfeQrF3NjLK8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:30+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" .
}