@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw> .
@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:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_head {
  this: np:hasAssertion dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion;
    np:hasProvenance dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance;
    np:hasPublicationInfo dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion a np:Assertion .
  
  dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance a np:Provenance .
  
  dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion {
  miriam-gene:1287 a ncit:C16612 .
  
  lld:C0241908 a ncit:C7057 .
  
  dgn-gda:DGNb8785cb45ae9e9ab5e610318af0fd6fc sio:SIO_000628 miriam-gene:1287, lld:C0241908;
    a sio:SIO_001121 .
}

dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_provenance {
  dgn-np:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_assertion dcterms:description
      "[This result suggests that COL4A5 should be added to the list of causative genes for benign familial hematuria, although the mechanism(s) by which the same mutation leads to the distinct phenotypes, i.e.]. 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:19937058;
    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:NP777702.RATA7dPt0t4FfWjRhjGn42BOI3e0IlrUYZXdaiUhR0bJw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:37+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" .
}