@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI> .
@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:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_head {
  this: np:hasAssertion dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_assertion;
    np:hasProvenance dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_provenance;
    np:hasPublicationInfo dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_assertion a np:Assertion .
  
  dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_provenance a np:Provenance .
  
  dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C1567741 a ncit:C7057 .
  
  dgn-gda:DGNe16d38b7430645f432c5fd2cf880409d sio:SIO_000628 miriam-gene:1287, lld:C1567741;
    a sio:SIO_001121 .
}

dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_provenance {
  dgn-np:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_assertion dcterms:description
      "[Recent genetic studies indicate that Alport syndrome and thin glomerular basement membrane disease (TMD) may both be due to COL4A3, COL4A4, and COL4A5 mutations, but there is continuing uncertainty concerning the diagnosis and management of patients without classic family history and symptoms.]. 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:12203217;
    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:NP366081.RANizq_mkSiR0kSCRqsLkbhy0RAQEz_YDTI7vOrf4ZQJI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:31+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" .
}