@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE> .
@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:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_head {
  this: np:hasAssertion dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_assertion;
    np:hasProvenance dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_provenance;
    np:hasPublicationInfo dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_assertion a np:Assertion .
  
  dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_provenance a np:Provenance .
  
  dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_assertion {
  miriam-gene:3084 a ncit:C16612 .
  
  lld:C2931876 a ncit:C7057 .
  
  dgn-gda:DGN2d76aa2e739780f8ae109cea7351a7b7 sio:SIO_000628 miriam-gene:3084, lld:C2931876;
    a sio:SIO_001121 .
}

dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_provenance {
  dgn-np:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_assertion dcterms:description
      "[To assess independent and joint effects between the different types of RET and NRG1 variants identified in HSCR patients, we used 254 Chinese sporadic HSCR patients and 143 ethnically matched controls for whom the RET and/or NRG1 variants genotypes (rare and common) were available.]. 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:23400839;
    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:NP709314.RAQIPG1_LIVzXy7ENv3jP7t3cfE3FlgYAUH1WQeiFP2gE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}