@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4> .
@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:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_head {
  this: np:hasAssertion dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion;
    np:hasProvenance dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance;
    np:hasPublicationInfo dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion a np:Assertion .
  
  dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance a np:Provenance .
  
  dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion {
  miriam-gene:5979 a ncit:C16612 .
  
  lld:C0025267 a ncit:C7057 .
  
  dgn-gda:DGNeaa8ae73b2e8dbee109b67356ce5c9a8 sio:SIO_000628 miriam-gene:5979, lld:C0025267;
    a sio:SIO_001121 .
}

dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance {
  dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion dcterms:description
      "[MEN1 gene mutation and RET codon 791 mutation in the same patient did not affect the typical phenotype of MEN1 or MEN2, and also the course of diseases seems to be unchanged.]. 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:15870131;
    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:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}