@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg> .
@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:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_head {
  this: np:hasAssertion dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_assertion;
    np:hasProvenance dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_provenance;
    np:hasPublicationInfo dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_assertion a np:Assertion .
  
  dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_provenance a np:Provenance .
  
  dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_assertion {
  miriam-gene:2312 a ncit:C16612 .
  
  lld:C0013595 a ncit:C7057 .
  
  dgn-gda:DGNbb7c4f977f3299c2d5430e64175ccaa1 sio:SIO_000628 miriam-gene:2312, lld:C0013595;
    a sio:SIO_001122 .
}

dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_provenance {
  dgn-np:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_assertion dcterms:description
      "[A group of 100 family trios (a total of 300 members with one affected AD proband and both parents) were recruited and screened for three filaggrin null mutations (3222del4, 3321delA and K4671X).]. 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:23152869;
    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:NP1028586.RAt51sDcNEHGN5qZpw1zbSYX-nWjNYMjHKVoB9wJ7Qtjg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:32+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" .
}