@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds> .
@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/v4.0.0/void/> .
dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_head {
  this: np:hasAssertion dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_assertion ;
    np:hasProvenance dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_provenance ;
    np:hasPublicationInfo dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_assertion a np:Assertion .
  dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_provenance a np:Provenance .
  dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_assertion {
  miriam-gene:1297 a ncit:C16612 .
  lld:C0154822 a ncit:C7057 .
  dgn-gda:DGN3f8f7c967279166b30d487fa48ec494a sio:SIO_000628 miriam-gene:1297 , lld:C0154822 ;
    a sio:SIO_001121 .
}
dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_provenance {
  dgn-np:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_assertion dcterms:description "[Although the overall phenotype was comparable to autosomal dominant Stickler, vitreous changes that may enable recognition of patients who are likely to carry mutations in COL9A1 were identified, and exudative retinal detachment was observed as a new finding in Stickler syndrome.]. 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:21421862 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP880985.RA3IVw5EFJ0IPTOQNmly-FC8cFmThZgkJDSrxGGypUqds130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:23+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}