@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0> .
@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:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_head {
  this: np:hasAssertion dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_assertion;
    np:hasProvenance dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_provenance;
    np:hasPublicationInfo dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_assertion a np:Assertion .
  
  dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_provenance a np:Provenance .
  
  dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0743098 a ncit:C7057 .
  
  dgn-gda:DGN92f63dc88164ee97c49d64c6cd012f01 sio:SIO_000628 miriam-gene:4000, lld:C0743098;
    a sio:SIO_001121 .
}

dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_provenance {
  dgn-np:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_assertion dcterms:description
      "[Lamin A/C mutations cause a series of human diseases, collectively called laminopathies, the most severe of which is Hutchinson Gilford progeria syndrome (HGPS) and restrictive dermopathy (RD) which arises due to an unsuccessful maturation of prelamin A.]. 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:18366013;
    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:NP832990.RA55Zgm-IIiUPA10jXRF8wNWXvjMd_lBH5NJFeZ251eY0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}