@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0> .
@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:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_head {
  this: np:hasAssertion dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_assertion ;
    np:hasProvenance dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_provenance ;
    np:hasPublicationInfo dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_assertion a np:Assertion .
  dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_provenance a np:Provenance .
  dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_assertion {
  miriam-gene:286887 a ncit:C16612 .
  lld:C2931923 a ncit:C7057 .
  dgn-gda:DGN8604359d070cd13b771517c2e0e9f1b8 sio:SIO_000628 miriam-gene:286887 , lld:C2931923 ;
    a sio:SIO_001122 .
}
dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_provenance {
  dgn-np:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_assertion dcterms:description "[have identified KRT6C mutations in patients with focal palmoplantar keratoderma (FPPK), but debate concerning overlapping phenotypes between FPPK and pachyonychia congenita (PC) will continue because only one family has nail involvement.]. 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:20081885 ;
    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:NP984758.RAxGEZzdSnOwsVzOS5MByi3f8-YCV0kvFmvSffQztyBx0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:42+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" .
}