@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4> .
@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:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_head {
  this: np:hasAssertion dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_assertion;
    np:hasProvenance dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_provenance;
    np:hasPublicationInfo dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_assertion a np:Assertion .
  
  dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_provenance a np:Provenance .
  
  dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_assertion {
  miriam-gene:2700 a ncit:C16612 .
  
  lld:C1858679 a ncit:C7057 .
  
  dgn-gda:DGN9848875dfcabbd32156a5fa91708aeb5 sio:SIO_000628 miriam-gene:2700, lld:C1858679;
    a sio:SIO_001121 .
}

dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_provenance {
  dgn-np:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_assertion dcterms:description
      "[These data confirm GJA3 as one of the most frequently mutated genes that underlie autosomal dominant cataract in humans, and further emphasize the importance of connexin function in maintaining lens transparency.]. 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:21897748;
    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:NP272292.RAe-wMHZZeUXE-JejsOALuc6pxs-E4ktYKlY1aku9Jvg4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:33+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" .
}