@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50> .
@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:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_head {
  this: np:hasAssertion dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion;
    np:hasProvenance dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_provenance;
    np:hasPublicationInfo dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion a np:Assertion .
  
  dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_provenance a np:Provenance .
  
  dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion {
  miriam-gene:5076 a ncit:C16612 .
  
  lld:C0042580 a ncit:C7057 .
  
  dgn-gda:DGNa3789ac8147573b236e95042ccb039de sio:SIO_000628 miriam-gene:5076, lld:C0042580;
    a sio:SIO_001121 .
}

dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_provenance {
  dgn-np:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_assertion dcterms:description
      "[We were unable to detect linkage to any of the genes and loci and could exclude the GDNF, RET, SLIT2, SPRY1, PAX2, AGTR2, UPK1A and UPK3A genes and the 1p13 and 20p13 loci from linkage to VUR.]. 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:17497182;
    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:NP524312.RAMxXTCBnM7sayeAwThdHel9X619XJ1DFNhQR0qfJaz50130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}