@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8> .
@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:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_head {
  this: np:hasAssertion dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_assertion;
    np:hasProvenance dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_provenance;
    np:hasPublicationInfo dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_assertion a np:Assertion .
  
  dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_provenance a np:Provenance .
  
  dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_assertion {
  miriam-gene:2668 a ncit:C16612 .
  
  lld:C2931876 a ncit:C7057 .
  
  dgn-gda:DGN1406afef21635952725f00909f117647 sio:SIO_000628 miriam-gene:2668, lld:C2931876;
    a sio:SIO_001121 .
}

dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_provenance {
  dgn-np:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_assertion dcterms:description
      "[These findings, together with the detection of sequence variants in PROKR1, PROK1 and PROKR2 genes associated to HSCR and, in some cases in combination with RET or GDNF mutations, provide the first evidence to consider them as susceptibility genes for HSCR.]. 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:21858136;
    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:NP167561.RAe6lWCF5DbxX0TQveFTXpgSCTJbtkfFPo80xsvOpZmD8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}