@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo> .
@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:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_head {
  this: np:hasAssertion dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_assertion;
    np:hasProvenance dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_provenance;
    np:hasPublicationInfo dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_assertion a np:Assertion .
  
  dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_provenance a np:Provenance .
  
  dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_assertion {
  miriam-gene:23418 a ncit:C16612 .
  
  lld:C0521683 a ncit:C7057 .
  
  dgn-gda:DGNfaee4542e75f21c1e84db98993b3d195 sio:SIO_000628 miriam-gene:23418, lld:C0521683;
    a sio:SIO_001121 .
}

dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_provenance {
  dgn-np:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_assertion dcterms:description
      "[Drusenlike deposits were more selectively observed in carriers with mutations in the AIPL1, CRB1, RPE65, and RPGRIP1 genes, whereas mild peripheral chorioretinal atrophy was only observed in AIPL1 and RPE65 carriers.]. 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:15691574;
    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:NP702538.RAoX4mE_TDfA5PYl9DhHEzRU8Fz0k2Udc3Q0pLEJplwNo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:07+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" .
}