@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4> .
@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:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_head {
  this: np:hasAssertion dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion;
    np:hasProvenance dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance;
    np:hasPublicationInfo dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion a np:Assertion .
  
  dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance a np:Provenance .
  
  dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion {
  miriam-gene:2260 a ncit:C16612 .
  
  lld:C0037274 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_provenance {
  dgn-np:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_assertion dcterms:description
      "[This review aims to summarize the current state of knowledge regarding the role of FLG mutations in ichthyosis vulgaris, atopic eczema, and other skin disorders, with an emphasis on potential clinical applications.]. 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:18620134;
    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:NP466762.RA2pd5UDgAL44jtEU_5adte0QMZSOQQMOiqaS8JRNezR4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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" .
}