@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q> .
@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:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_head {
  this: np:hasAssertion dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion;
    np:hasProvenance dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance;
    np:hasPublicationInfo dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion a np:Assertion .
  
  dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance a np:Provenance .
  
  dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion {
  miriam-gene:100128922 a ncit:C16612 .
  
  lld:C0011053 a ncit:C7057 .
  
  dgn-gda:DGNaf553e69965800e202972e24e0815930 sio:SIO_000628 miriam-gene:100128922,
      lld:C0011053;
    a sio:SIO_001121 .
}

dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_provenance {
  dgn-np:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_assertion dcterms:description
      "[It is important to consider connexin deafness in any child with recessive nonsyndromic hearing loss as well as simplex cases with no history of other affected family members even when the newborn hearing screening results were within the normal range.]. 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:17086082;
    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:NP221100.RAUMUEl3bs8ixUPXcr4E4wpNTYzEy-IcX_TFz5m24qi3Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}