@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY> .
@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:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_head {
  this: np:hasAssertion dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_assertion;
    np:hasProvenance dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_provenance;
    np:hasPublicationInfo dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_assertion a np:Assertion .
  
  dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_provenance a np:Provenance .
  
  dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGN3748baadbf1042885311492c1f964109 sio:SIO_000628 miriam-gene:4000, lld:C0242339;
    a sio:SIO_001121 .
}

dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_provenance {
  dgn-np:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_assertion dcterms:description
      "[FPLD was recently discovered to result from mutated LMNA (R482Q; OMIM #150330.0010), which is the gene encoding nuclear lamins A and C. Results from extended pedigrees indicate that dyslipidemia precedes the plasma glucose abnormalities in FPLD subjects with mutant LMNA, and that the hyperinsulinemia is present early in the course of the disease.]. 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:11122771;
    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:NP377127.RAF1_sfww4Zb628AS4EYRm7mPqNVfwpMrgaKfGebj_fxY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}