@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM> .
@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:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_head {
  this: np:hasAssertion dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion;
    np:hasProvenance dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance;
    np:hasPublicationInfo dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion a np:Assertion .
  
  dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance a np:Provenance .
  
  dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion {
  miriam-gene:4638 a ncit:C16612 .
  
  lld:C1290884 a ncit:C7057 .
  
  dgn-gda:DGNe0d32d4b5b94b8d69e1fc07466372098 sio:SIO_000628 miriam-gene:4638, lld:C1290884;
    a sio:SIO_001121 .
}

dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_provenance {
  dgn-np:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_assertion dcterms:description
      "[These functional insights into the involvement of intronic MYLK SNPs further strengthen the concept that MYLK contributes to inflammatory disease susceptibility and represents an attractive molecular target in complex inflammatory disorders.]. 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:22015949;
    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:NP449885.RACcQOsPAYnEsLv-BAakKDl2wFOMHmriDSC0dLrcU45eM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:28+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" .
}