@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY> .
@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:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_head {
  this: np:hasAssertion dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_assertion;
    np:hasProvenance dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_provenance;
    np:hasPublicationInfo dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_assertion a np:Assertion .
  
  dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_provenance a np:Provenance .
  
  dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C0017636 a ncit:C7057 .
  
  dgn-gda:DGN69730800225d74948fc06de68a605563 sio:SIO_000628 miriam-gene:1287, lld:C0017636;
    a sio:SIO_001121 .
}

dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_provenance {
  dgn-np:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_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:NP778108.RA5xMcnXyMscTxZ6oSAqTCM1-1zjN2BNfRTa55nfy0iaY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:51+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" .
}