@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg> .
@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:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_head {
   this: np:hasAssertion dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_assertion ;
    np:hasProvenance dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_provenance ;
    np:hasPublicationInfo dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_assertion a np:Assertion .
  dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_provenance a np:Provenance .
  dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_assertion {
   miriam-gene:1913 a ncit:C16612 .
  lld:C0013575 a ncit:C7057 .
  dgn-gda:DGN1567a51faf2b2bd97224785ba0c15b8e sio:SIO_000628 miriam-gene:1913 , lld:C0013575 ;
    a sio:SIO_001121 .
}
dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_provenance {
   dgn-np:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_assertion dcterms:description "[p63 mutations have been associated with several human hereditary disorders characterized by ectodermal dysplasia such as EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome, ADULT (acro, dermato, ungual, lacrimal, tooth) syndrome and AEC (ankyloblepharon, ectodermal dysplasia, clefting) syndrome (also called Hay-Wells syndrome).]. 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:16319531 ;
    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:NP365928.RASiMzE-C7dfzqLXhhH75foKCdTqurhqMPHNg9gApmIXg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:41:11+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" .
}