@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs> .
@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:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_head {
  this: np:hasAssertion dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_assertion;
    np:hasProvenance dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_provenance;
    np:hasPublicationInfo dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_assertion a np:Assertion .
  
  dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_provenance a np:Provenance .
  
  dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C1621958 a ncit:C7057 .
  
  dgn-gda:DGN734c15fba7c6044e96c75a7b9e46411e sio:SIO_000628 miriam-gene:1287, lld:C1621958;
    a sio:SIO_001121 .
}

dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_provenance {
  dgn-np:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_assertion dcterms:description
      "[Alport Syndrome (AS) is an inherited progressive disease that is caused by mutations of the genes encoding the key collagen chains, α3, α4, and α5, which are necessary for the composition of collagen type IV to form a robust glomerular basement membrane (GBM), capable of withstanding the significant biomechanical strain to which the glomerulus is subjected.]. 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:22903660;
    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:NP683412.RA5OKIALOnHIRqnW02EXDyykMh_uaAEZiEmi4ZBw_vuUs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}