@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0> .
@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:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_head {
  this: np:hasAssertion dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_assertion;
    np:hasProvenance dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_provenance;
    np:hasPublicationInfo dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_assertion a np:Assertion .
  
  dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_provenance a np:Provenance .
  
  dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_assertion {
  miriam-gene:2312 a ncit:C16612 .
  
  lld:C0011603 a ncit:C7057 .
  
  dgn-gda:DGNfd85cd724efa86dec6ce3807004f80b5 sio:SIO_000628 miriam-gene:2312, lld:C0011603;
    a sio:SIO_001121 .
}

dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_provenance {
  dgn-np:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_assertion dcterms:description
      "[In our clinic, we have observed a distinct phenotype of hand eczema in patients with filaggrin mutation carrier status, characterized by fissured dermatitis on the dorsal aspect of the hands and with only sparse involvement of the palms including fine scaling.]. 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:21777221;
    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:NP917491.RAuxqMl85sgw3c_ZZFnrwCgcZmp-cy5HnLSz-qDk7tRB0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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" .
}