@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI> .
@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/v3.0.0/void/> .

dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_head {
  this: np:hasAssertion dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_assertion;
    np:hasProvenance dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_provenance;
    np:hasPublicationInfo dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_assertion a np:Assertion .
  
  dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_provenance a np:Provenance .
  
  dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_assertion {
  miriam-gene:6445 a ncit:C16612 .
  
  lld:C0020757 a ncit:C7057 .
  
  dgn-gda:DGNd95cd67077b20fef2e4c329f29765c9e sio:SIO_000628 miriam-gene:6445, lld:C0020757;
    a sio:SIO_001121 .
}

dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_provenance {
  dgn-np:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_assertion dcterms:description
      "[The nature of the wild-type gene product at the mouse ichthyosis (ic) locus has been of great interest because mutations at this locus cause marked abnormalities in nuclear heterochromatin, similar to those observed in Pelger-Huët anomaly (PHA).]. 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:12490533;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP692299.RADPDO687yH7CoFu17cAv7Q1VJTHl8fgRWZJ7j2CPoFkI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:37+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}