@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho> .
@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:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_head {
  this: np:hasAssertion dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_assertion;
    np:hasProvenance dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_provenance;
    np:hasPublicationInfo dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_assertion a np:Assertion .
  
  dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_provenance a np:Provenance .
  
  dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_assertion {
  miriam-gene:2675 a ncit:C16612 .
  
  lld:C0549473 a ncit:C7057 .
  
  dgn-gda:DGN344dafb8950bfa58352f551f5b4369b5 sio:SIO_000628 miriam-gene:2675, lld:C0549473;
    a sio:SIO_001122 .
}

dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_provenance {
  dgn-np:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_assertion dcterms:description
      "[Our results show that no statistical signification was found when Spanish sMTC patients were compared to controls. Taken together with the observations in the German sMTC series, the present findings suggest that GFRA1-193C > G and 537T > C could be in linkage disequilibrium with other loci responsible for the disease with a founder effect in Germany. Alternatively, the combined observations might also suggest that, if indeed the polymorphisms are functional, the effect is small.]. 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:12490080;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP60374.RA-W-eIwTSaPCh1IlGaITy0v9jcnimrcepp_9awgZcyho130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}