@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I> .
@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:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_head {
  this: np:hasAssertion dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion ;
    np:hasProvenance dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance ;
    np:hasPublicationInfo dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion a np:Assertion .
  dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance a np:Provenance .
  dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion {
  miriam-gene:7431 a ncit:C16612 .
  lld:C0079298 a ncit:C7057 .
  dgn-gda:DGN5ae888075a10cbd26b7e089cf2f7f8e4 sio:SIO_000628 miriam-gene:7431 , lld:C0079298 ;
    a sio:SIO_001121 .
}
dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_provenance {
  dgn-np:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_assertion dcterms:description "[Further, to explore possible correlations with function, the structural effects of the mutations in segment 2B of KRT5 and KRT14 and associated with EBS in our patients, as well as those reported previously, were modelled by molecular dynamics with the aid of the known crystal structure of the analogous segment of human vimentin.]. 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:20030639 ;
    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:NP652545.RAwUHDgsg7WfjLwF8RJdWL1n1URZVhkKZCedXBSqPm2_I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:33+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> ;
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}