@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM> .
@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:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_head {
  this: np:hasAssertion dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_assertion;
    np:hasProvenance dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_provenance;
    np:hasPublicationInfo dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_assertion a np:Assertion .
  
  dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_provenance a np:Provenance .
  
  dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_assertion {
  miriam-gene:2312 a ncit:C16612 .
  
  lld:C0037274 a ncit:C7057 .
  
  dgn-gda:DGN9525985f19e1c0f2d65817af2406ce8e sio:SIO_000628 miriam-gene:2312, lld:C0037274;
    a sio:SIO_001122 .
}

dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_provenance {
  dgn-np:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_assertion dcterms:description
      "[Recently, 2 loss-of-function mutations (R501X and 2282derl4) in the filaggrin gene (FLG) that cause ichthyosis vulgaris, one of the most common inherited skin disorders of keratinization, have been reported to be strong predisposing factors for AD.]. 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:16815158;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP557590.RAc1jLkzrMnKI1eF29__xOiub8weImkVfNHsgZoQO1wkM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:57+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" .
}