@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM> .
@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:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_head {
  this: np:hasAssertion dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion;
    np:hasProvenance dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance;
    np:hasPublicationInfo dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion a np:Assertion .
  
  dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance a np:Provenance .
  
  dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion {
  miriam-gene:4988 a ncit:C16612 .
  
  lld:C0027708 a ncit:C7057 .
  
  dgn-gda:DGNd589256f8e0f19ae20304eb22d151529 sio:SIO_000628 miriam-gene:4988, lld:C0027708;
    a sio:SIO_001121 .
}

dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance {
  dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion dcterms:description
      "[On the basis of our male patient 1 and on further six male cases of the literature, we also highlighted that larger 19q13.11 deletions including the Wilms tumor interacting protein (WTIP) gene, proximal to the MOR, results in hypospadias making this gene a possible candidate for this genital abnormality due to its well-known interaction with WT1.]. 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:22378287;
    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:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}