@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_head {
  this: np:hasAssertion dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_assertion ;
    np:hasProvenance dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_provenance ;
    np:hasPublicationInfo dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_assertion a np:Assertion .
  dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_provenance a np:Provenance .
  dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_assertion {
  miriam-gene:3000 a ncit:C16612 .
  lld:C0035334 a ncit:C7057 .
  dgn-gda:DGN91a56e12b37612e8e4a0b18214c4d649 sio:SIO_000628 miriam-gene:3000 , lld:C0035334 ;
    a sio:SIO_001122 .
}
dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_provenance {
  dgn-np:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_assertion dcterms:description "[TIMP3 novel variants were found in two SFD patients, PRPH2 variants in 14 PD patients, ABCA4 variants in four PD patients, and p.Arg838His GUCY2D mutation in six patients diagnosed with dominant CRD; one patient additionally had a CRX VUS.]. 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:25082885 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP442496.RAIHEBI6djgaHfRb-tqTo6-ACz61YeAJmFnamgTnMjomI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:58+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}