@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw> .
@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:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_head {
  this: np:hasAssertion dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_assertion;
    np:hasProvenance dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_provenance;
    np:hasPublicationInfo dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_assertion a np:Assertion .
  
  dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_provenance a np:Provenance .
  
  dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_assertion {
  miriam-gene:1915 a ncit:C16612 .
  
  lld:C0271097 a ncit:C7057 .
  
  dgn-gda:DGN2e7668c34d74ff9b0c3272a14908318a sio:SIO_000628 miriam-gene:1915, lld:C0271097;
    a sio:SIO_001121 .
}

dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_provenance {
  dgn-np:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_assertion dcterms:description
      "[Several of the top candidate genes include EEF1A1, ROBO1, PLXNA4, SLIT3, NRP1, and NOTCH2, as well as genes associated with the Usher syndrome, PCDH15 and USH2A, and are plausible candidates contributing to the developmental defects in Gbx2(-/-) mice.]. 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:23144817;
    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:NP624686.RAZ3PgXfgIlnCfkszhltqw4dJwsFLLXxtArZmjlsw6tPw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:17+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" .
}