@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k> .
@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:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_head {
  this: np:hasAssertion dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_assertion;
    np:hasProvenance dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_provenance;
    np:hasPublicationInfo dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_assertion a np:Assertion .
  
  dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_provenance a np:Provenance .
  
  dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C1280433 a ncit:C7057 .
  
  dgn-gda:DGN044a754480cbf491f12e42d4f692c872 sio:SIO_000628 miriam-gene:4000, lld:C1280433;
    a sio:SIO_001121 .
}

dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_provenance {
  dgn-np:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_assertion dcterms:description
      "[Genetic forms of partial lipodystrophy are currently recognized as two syndromes with subcutaneous lipoatrophy but preserved or increased fat at the level of face and neck (Dunnigan syndrome or FPLD due to LMNA mutations) and/or abdomen (PPARgamma-linked forms) and are both transmitted as dominant diseases.]. 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:15773753;
    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:NP922943.RAlg1hJoAO3eVIX7FdX3WRXKgYpUXq7IckpW8zyOtSl2k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:26+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" .
}