@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY> .
@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:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_head {
  this: np:hasAssertion dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_assertion;
    np:hasProvenance dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_provenance;
    np:hasPublicationInfo dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_assertion a np:Assertion .
  
  dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_provenance a np:Provenance .
  
  dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C1567741 a ncit:C7057 .
  
  dgn-gda:DGN01e7208bc941a6b0291f73546bc2d0e6 sio:SIO_000628 miriam-gene:1287, lld:C1567741;
    a sio:SIO_001121 .
}

dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_provenance {
  dgn-np:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_assertion dcterms:description
      "[Genetic diseases affecting laminin and type IV collagen synthesis also are presented, with an emphasis on mutations to LAMB2 (Pierson syndrome) and COL4A3, COL4A4, and COL4A5 (Alport syndrome), and their experimental mouse models.]. 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:22958488;
    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:NP320155.RAv2i6dK0csuktmv5VV_KxFxYq8kWVqNSrYijFJL0RLvY130_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" .
}