@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo> .
@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:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_head {
  this: np:hasAssertion dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_assertion ;
    np:hasProvenance dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_provenance ;
    np:hasPublicationInfo dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_assertion a np:Assertion .
  dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_provenance a np:Provenance .
  dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_assertion {
  miriam-gene:1285 a ncit:C16612 .
  lld:C1565489 a ncit:C7057 .
  dgn-gda:DGN2c1daa3f9b9d5391c3972fd570e5d633 sio:SIO_000628 miriam-gene:1285 , lld:C1565489 ;
    a sio:SIO_001121 .
}
dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_provenance {
  dgn-np:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_assertion dcterms:description "[It is unclear whether individuals with TBMN and impaired renal function represent part of the spectrum of TBMN associated with heterozygous COL4A3 or COL4A4 mutations, or if their disease is caused by mutations of other genes, or whether it is caused by a second coexistent renal lesion or is misdiagnosed Alport 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:15880323 ;
    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:NP319925.RADIKPE8ZAoXjAcc0FybTIL22Yzq61_p_UkZaxjI_96Qo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:44+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" .
}