@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk> .
@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:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_head {
  this: np:hasAssertion dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_assertion;
    np:hasProvenance dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_provenance;
    np:hasPublicationInfo dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_assertion a np:Assertion .
  
  dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_provenance a np:Provenance .
  
  dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0033300 a ncit:C7057 .
  
  dgn-gda:DGN28ae2f841703c35d5498fe5121cabe07 sio:SIO_000628 miriam-gene:4000, lld:C0033300;
    a sio:SIO_001121 .
}

dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_provenance {
  dgn-np:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_assertion dcterms:description
      "[Moreover, the well-known disease called Hutchinson-Gilford Progeria Syndrome due to extensive mutations in LMNA gene, in addition to the systemic phenotype of premature aging, is characterised by the death of patients at around 13 typically for a heart attack or stroke, suggesting again the heart as the main site sensitive to Lamin A/C disfunction.]. 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:25055884;
    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:NP1204410.RARPa-iV6JZ7U4T5wKVFykOjYO624wzAahl2R_QWgXfHk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:52+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" .
}